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Clinical and Dermoscopic Features of Fungal Melanonychia: Differentiating from Subungual Melanoma

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Background: Fungal melanonychia (FM) is a rare nail disorder that presents as dark pigmentation in the nail plate because of fungal nail infection. The diagnosis of FM is occasionally confusing because its appearance is similar to melanonychia due to other causes including malignant melanoma. Dermoscopy could help increase the accuracy of diagnosing the cause of pigmented nail lesions. However, dermoscopic features of FM are not well elucidated. Objective: This study aimed to investigate clinical and dermoscopic characteristics of FM. Methods: The clinical features and dermoscopic findings of 20 patients diagnosed with FM and 14 patients diagnosed with subungual melanoma the Department of Dermatology of Pusan National University Hospitals (Busan and Yangsan) were retrospectively reviewed. Results: FM mainly occurred as a solitary form in the toenail. Patients in the FM group were older than those in the subungual melanoma group. The most distinguishable general dermoscopic features in FM were a distal diffuse pattern, distal linear pattern, and light brown to yellowish color. FM-associated specific dermoscopic patterns such as the reverse triangular pattern, subungual hyperkeratosis, scale on the nail surface, and white or yellowish streaks were dominantly observed in the FM group compared to the subungual melanoma group. Conclusion: FM-associated dermoscopic patterns and distal diffuse and linear patterns could be helpful diagnostic clues for differential diagnosis of FM from subungual melanoma.
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HJ Kim, et al
460
Ann Dermatol
Received June 3, 2019, Revised May 22, 2020, Accepted for publication
May 22, 2020
Corresponding author: Hyun-Chang Ko, Department of Dermatology, Pusan
National University Yangsan Hospital, 20 Geumo-ro, Mulgeum-eup, Yangsan
50612, Korea. Tel: 82-55-360-1678, Fax: 82-55-360-1679, E-mail: hcko@
pusan.ac.kr
ORCID: https://orcid.org/0000-0002-3459-5474
T
his is an Open Access article distributed under the terms of the Creative
Commons Attribution Non-Commercial License (http://creativecommons.
org/licenses/by-nc/4.0) which permits unrestricted non-commercial use,
distribution, and reproduction in any medium, provided the original work
is properly cited.
Copyright © The Korean Dermatological Association and The Korean
Society for Investigative Dermatology
pISSN 1013-9087eISSN 2005-3894
Ann Dermatol Vol. 32, No. 6, 2020 https://doi.org/10.5021/ad.2020.32.6.460
ORIGINAL ARTICLE
Clinical and Dermoscopic Features of Fungal
Melanonychia: Differentiating from Subungual
Melanoma
Hak-Jun Kim1,2, Tae-Wook Kim1,2, Sung-Min Park1,2, Hyun-Joo Lee1, Gun-Wook Kim1,
Hoon-Soo Kim1, Byung-Soo Kim1, Moon-Bum Kim1, Hyun-Chang Ko1,2
1Department of Dermatology, Pusan National University Hospital, Busan, 2Department of Dermatology, Pusan National University
Yangsan Hospital, Yangsan, Korea
Background: Fungal melanonychia (FM) is a rare nail dis-
order that presents as dark pigmentation in the nail plate be-
cause of fungal nail infection. The diagnosis of FM is occa-
sionally confusing because its appearance is similar to mela-
nonychia due to other causes including malignant melanoma.
Dermoscopy could help increase the accuracy of diagnosing
the cause of pigmented nail lesions. However, dermoscopic
features of FM are not well elucidated. Objective: This study
aimed to investigate clinical and dermoscopic character-
istics of FM. Methods: The clinical features and dermoscopic
findings of 20 patients diagnosed with FM and 14 patients di-
agnosed with subungual melanoma the Department of
Dermatology of Pusan National University Hospitals (Busan
and Yangsan) were retrospectively reviewed. Results: FM
mainly occurred as a solitary form in the toenail. Patients in
the FM group were older than those in the subungual mela-
noma group. The most distinguishable general dermoscopic
features in FM were a distal diffuse pattern, distal linear pat-
tern, and light brown to yellowish color. FM-associated spe-
cific dermoscopic patterns such as the reverse triangular pat-
tern, subungual hyperkeratosis, scale on the nail surface, and
white or yellowish streaks were dominantly observed in the
FM group compared to the subungual melanoma group.
Conclusion: FM-associated dermoscopic patterns and distal
diffuse and linear patterns could be helpful diagnostic clues
for differential diagnosis of FM from subungual melanoma.
(Ann Dermatol 32(6) 460465, 2020)
-Keywords-
Dermoscopy, Fungal melanonychia, Subungual melanoma
INTRODUCTION
Fungal melanonychia (FM) is a rare nail disorder that pres-
ents with dark to brown pigmentation due to fungal in-
fection of the nails. It is mainly caused by dematiaceous
fungi and, rarely, by yeasts and non-dermatophyte fungi1.
The diagnosis of FM is occasionally difficult because it
may clinically mimic melanonychia due to other causes,
such as melanocytic nevus and subungual melanoma.
Recently, dermoscopy has been used to improve the accu-
racy of diagnosing the cause of pigmented nail lesions. A
few studies have evaluated the dermoscopic features of
FM2,3. However, these studies were limited by a small
sample size or the absence of control groups. Here, we
aimed to identify the clinical and dermoscopic character-
istics of FM to enhance the accuracy of diagnosis. In this
study, we have compared clinical and dermoscopic fea-
tures of FM with those of subungual melanoma.
Characteristic Features of Fungal Melanonychia
Vol. 32, No. 6, 2020
461
Fig. 1. The general shapes of mela-
nonychia that were analyzed in this
study; (A) longitudinal, (B) distal li-
near, (C) total diffuse, and (D) distal
diffuse pattern.
MATERIALS AND METHODS
Study population
Of the patients with FM who visited the Department of
Dermatology of Pusan National University Hospitals (Busan
and Yangsan), South Korea from December 2014 to August
2018, a total of 20 patients who had dermoscopic records
were included in this study. The diagnosis of FM was made
based on clinical presentations and a mycological test. A
potassium hydroxide (KOH) smear test was performed in
all patients, and only patients with positive test results were
enrolled. Fungal culture was not always performed because
of its low sensitivity and long incubation period. The con-
trol group comprised all patients diagnosed with subun-
gual melanoma with dermoscopic records during the same
period. Subungual melanoma was diagnosed by histopatho-
logical findings. Of the 14 patients who had subungual
melanoma, 4 had invasive melanoma. All subungual mel-
anomas were confirmed by a negative KOH smear test and
excluded accompanying fungal infection. The study was
exempted from the requirement for approval by the ethics
committee of Pusan National University Yangsan Hospital
(IRB no. 05-2019-057), and informed consent was obtained
from the patients included in this study.
We received the patient’s consent form about publishing
all photographic materials.
Method
Data from the medical records of patients were used to in-
vestigate the clinical characteristics of the patients (age,
sex, number of lesions, location, involved area, duration,
and comorbidities). Clinical photographs were taken with
a camera (EOS 50D; Canon, Tokyo, Japan). Dermoscopic
images were acquired using a dermoscope (DermLite II
PRO HR or DermLite II DL3; 3Gen, San Juan Capistrano,
CA, USA) that was equipped with a digital camera (CyberShot
DSC W-290; Sony Co, Tokyo, Japan).
All data were analyzed using IBM SPSS Statistics ver. 22.0
(IBM Corp., Armonk, NY, USA). p-values of less than 0.05
were considered significant.
Evaluation of dermoscopic features
General dermoscopic features (color and general shape)
were investigated. The color of the nail lesion was divided
into black, dark brown, light brown, yellow, gray, and red
categories. The general shape of the melanonychia was clas-
sified as longitudinal, distal diffuse, proximal diffuse, distal
linear, and total diffuse patterns (Fig. 1). FM-associated der-
moscopic patterns, including reverse triangular shapes, sub-
ungual hyperkeratosis, scales on the nail surfaces, and yel-
HJ Kim, et al
462
Ann Dermatol
Fig. 2. The fungal melanonychia-
associated dermoscopic patterns. (A)
Reverse triangular shape (yellow
asterisks), (B) subungual hyperkera-
tosis (whitish arrow), (C) scales on
the nail surface (red arrows), and
(D) yellowish streaks (yellow circle).
Table 1. Sociodemographic and clinical features of fungal
melanonychia (FM group) and subungual melanoma (control
group)
Feature FM group
(n=20)
Control group
(n=14) p-value
Age of onset (yr) 57.2 (30~87) 55.1 (42~78) 0.05
Sex
Male 10 6 0.062
Female 10 8
Location
Finger:toe 6:16 9:5 0.05
Right:left 11:9 8:6 0.133
Mean no. of
nails involved
1.1 1.0 0.674
Involved area (%) 27.3 38.7 0.05
Duration (mo) 18.2 20.8 0.088
Comorbidity
Hypertension 9 8
Diabetes 7 6
Dyslipidemia 4 5
Cancer 3 3
Others 2 3
Values are presented as mean (range) or number only.
lowish streaks, were evaluated (Fig. 2). Melanoma-asso-
ciated patterns, such as Hutchinson’s nail sign, irregularity,
nail plate destruction, the triangular sign, and ulceration,
were also evaluated to find a diagnostic clue that differ-
entiates FM from subungual melanoma.
RESULTS
Sociodemographic and clinical features
The sociodemographic and clinical information of the FM
and control groups (the subungual melanoma group) are
presented in Table 1. We reviewed 34 patients (20 pa-
tients with FM and 14 patients with subungual melano-
ma). The mean age was 57.2 and 55.1 years in the FM
and the subungual melanoma groups, respectively. The
male-to-female ratio was 1:1 and 1:1.8 in the FM and sub-
ungual melanoma groups, respectively. FM occurred on
1.1 nail units per patient, and subungual melanoma oc-
curred on 1.0 nail units per patient. The involved nail area
of the FM group was smaller than that of the control group
(27.3% in FM, 38.7% in subungual melanoma, p0.05).
There was no significant difference in incidence rates be-
tween the left side and the right side of the body. FM oc-
curred in the toenails three times more often than in the
Characteristic Features of Fungal Melanonychia
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463
Table 2. General dermoscopic features of fungal melanonychia
(FM group) and subungual melanoma (control group)
General dermo-
scopic feature
FM group
(n=20)
Control group
(n=14) p-value
Color
Black 10 (50.0) 6 (42.9) 0.231
Dark brown 9 (45.0) 8 (57.1) 0.177
Light brown 9 (45.0) 0 (0) 0.05
Yellow 8 (40.0) 0 (0) 0.05
Gray 0 (0) 0 (0) -
Red 0 (0) 0 (0) -
Multicolored
pattern
(2 colors)
13 (65.0) 11 (78.6) 0.159
General pattern
Longitudinal 6 (30.0) 6 (42.9) 0.056
Distal diffuse 7 (35.0) 0 (0) 0.05
Proximal diffuse 1 (5.0) 2 (14.3) 0.088
Distal linear 4 (20.0) 0 (0) 0.05
Total diffuse 2 (10.0) 5 (35.7) 0.05
Values are presented as number (%). -: not available.
Table 3. Specific dermoscopic features of fungal melanonychia
(FM group) and subungual melanoma (control group)
Specific dermo-
scopic feature
FM group
(n=20)
Control group
(n=14) p-value
FM associated pattern
Reverse
triangular shape
10 (50.0) 0 (0) 0.05
Subungual
hyperkeratosis
7 (35.0) 2 (14.3) 0.05
Scales on
the nail surface
14 (70.0) 8 (57.1) 0.05
White or
yellow streak
18 (90.0) 0 (0) 0.05
MM associated pattern
Hutchinson sign 0 (0) 8 (57.1) 0.05
Pseudo-Hutchins
on sign
0 (0) 4 (28.6) 0.05
Nail plate
destruction
5 (25.0) 4 (28.6) 0.312
Triangular sign 0 (0) 5 (35.7) 0.05
Dots/globules 4 (20.0) 7 (50.0) 0.05
Ulceration 0 (0) 2 (14.3) 0.05
Values are presented as number (%). MM: malignant melanoma.
fingernails. The most common onset site of FM was the
first toe (55.0%), followed by the first finger (15.0%), and
the second toe (10.0%). In contrast, subungual melanoma
nail lesions were found predominantly in the fingernails
and mainly occurred in the second finger (35.7%), first fin-
ger (28.6%), and first toe (14.3%). There was no signifi-
cant difference in the disease duration between the two
groups. Hypertension was the most common comorbidity
in both groups, followed by diabetes and dyslipidemia.
Dermoscopic features
The general dermoscopic characteristics, such as color and
shape of the melanonychia, are summarized in Table 2. In
the FM group, the most common color was black (50.0%),
followed by dark brown (45.0%), light brown (45.0%),
and yellow (40.0%). In the control group, the most com-
mon colors were dark brown (57.1%) and black (42.9%).
Although black and dark brown were the predominant
colors in both groups, the proportion of yellow melano-
nychia was significantly higher in the FM group than in
the control group (40.0% vs. 0%). The most common FM
pattern was a distal diffuse type of melanonychia (35.0%).
Other common patterns included the longitudinal (30.0%),
distal linear (20.0%), and total diffuse (10.0%) types of
melanonychia. Among these, the distal diffuse and linear
patterns were more distinctive in the FM group than in the
control group (p0.05). Statistical analyses between the
FM and subungual melanoma groups were performed to
identify specific dermoscopic differences (Table 3). We
analyzed the following four FM-associated dermoscopic
patterns: white or yellow streaks, reverse triangular pat-
terns, subungual hyperkeratosis, and scales on the nail
surfaces. In this study, we observed that all four features
were positive predictors of FM (Fig. 2). In contrast, mela-
noma-associated patterns, such as Hutchinson’s sign, pseudo-
Hutchinson’s sign, the triangular sign, nail plate destruc-
tion, dots/globules, and ulceration, were negative predictors
of FM compared with the subungual melanoma (p0.05).
DISCUSSION
Melanonychia is defined by dark pigmentations in the nail
unit. There are many different causes of melanonychia,
ranging from nail matrix nevus, melanocytic activation due
to drug use or trauma, subungual hemorrhage, and infec-
tion to malignant melanoma. Some of these causes have
unique presentations, which make them easy to distinguish.
However, most cases of melanonychia are difficult to dis-
tinguish because of their similar clinical presentations4,5.
FM is a rare nail disorder that presents with dark to brown
pigmentation on the nail plate because of fungal nail
infection. Some species of fungi can synthesize melanin.
Unlike human melanin, which is derived from tyrosine,
fungal melanin is synthesized via the pentaketide pathway.
The fungal melanin serves as a barrier that protects the
fungus from environmental stresses, such as temperature,
HJ Kim, et al
464
Ann Dermatol
radiation, and the host’s immune system. In addition, mel-
anin-synthesizing fungi are more resistant to ultraviolet
and X-ray radiation and extreme temperatures compared
to other fungi. Among the many species of fungi, the most
frequently isolated fungi in FM are Trichophyton rubrum,
a nondematiaceous dermatophyte, and Scytalidium dimi-
diatum, a dematiaceous fungi1,6. However, no analysis
was made about causative organisms in this study because
fungal culture was not routinely performed. Further stud-
ies will be needed to investigate characteristic patterns of
FM based on specific causative pathogens.
We compared the clinical and dermoscopic features of
FM with subungual melanoma to find diagnostic differ-
ences between the groups. The clinical features showed
that the onset age of FM was relative older than that of the
control. The mean age of FM was 57.2 years, which was
significantly higher than that of individuals in the control
group (55.1 years). FM showed a tendency to develop in a
single nail unit (1.1 nail units per patients). However,
some patients with a solitary FM lesion had multiple nail
unit (mean 3.67) involvement of onychomycosis. In a
study of 1897 Korean patients with onychomycosis, 31.3%
of patients showed multiple nail involvement (i.e., more
than 5 nail units involved)7. In contrast, multiple nail in-
volvement of FM was rarely observed in this study, with
only one patient showing FM of multiple nails. This sug-
gested that the incidence of FM is relatively low compared
to onychomycosis. Furthermore, in previous studies, most
cases of onychomycosis (93.8%) involved toenails, and
only 2.2% of the cases involved fingernails7. Similarly, FM
occurred three times more often in toenails (72.7%) than
in fingernails (27.2%) in this study. However, subungual
melanoma was mainly observed in fingernails (64.3%). To
summarize the clinical analysis, FM tends to occur as a
solitary lesion in the great toe, and its mean age of onset
was higher than in cases of subungual melanoma.
Dermoscopy is a useful noninvasive tool that has been re-
ported to improve diagnostic accuracy of nail pigmentation.
Reports on the dermoscopic features of FM are scarce, and
only a few original studies on FM have been reported2,8.
Kilinc Karaarslan et al.3 have described the dermoscopic
patterns in 14 cases of FM and suggested that multicolored
pigmentation and reverse triangular patterns are distinctive
features of FM. Hirata et al.9 have also reported a case of
FM; they dermoscopically described it as a brown nail
background with regular black lines. However, these stud-
ies were limited by a small sample size and the absence of
a control group. Ohn et al.2 have reported the first com-
prehensive comparative analysis of dermoscopic findings
between FM and other melanonychia caused by nail ma-
trix nevus, melanocytic activation, and subungual melanoma.
Their study revealed that several dermoscopic features,
such as reverse triangular patterns, subungual hyper-
keratosis, and white or yellow streaks, were characteristics
of FM. In this study, we observed that all these patterns
were predominantly observed in FM cases. Among these
patterns, white or yellow streaks and reverse triangular pat-
terns were the most distinctive features of FM. Black pig-
mentation was the predominant color in the control group.
This study also showed that the yellow color was a pos-
itive indicator for FM. Ohn et al.2 suggested that multi-
colored patterns were characteristic of FM. However, this
study showed no significant difference in the presence of
multicolored patterns between the FM and control groups.
We chose cases of subungual melanoma as the control
group because it usually has a heterogenous clinical pre-
sentation. The most common general pattern of dermo-
scopic findings in FM was the distal diffuse pattern (35.0%),
followed by the longitudinal (30.0%) and distal linear (20.0%)
patterns. The two distal patterns were indicators of FM (p
0.05), but the longitudinal pattern was not. The longitudi-
nal pattern was the predominant pattern in the control
group (42.9%). Two distal patterns that were not presented
in the previous report were identified as characteristic FM
dermoscopic findings in this study.
Piraccini et al.10 have reported that irregular white to yel-
low pigmentation and a “jagged edge” with sharp longi-
tudinal whitish indentations are specific features of FM. In
some previous studies, the spike or streak were useful in-
dicators of fungal invasion of the nail plate. In this study,
we used the term “white or yellow streak,” and this pat-
tern was more frequently observed in the FM group (90.0%)
than in the control group (0%). The reverse triangular pat-
tern is caused by fungal invasion from the distal nail
plate11, and our data showed that this pattern was preva-
lent in the FM group (50.0%), but not in the melanoma
group (0%).
Subungual melanoma should always be included in the
differential diagnosis of FM because melanoma is a life-
threatening disorder. FM could mimic subungual melano-
ma because it can present as a brown-black melanonychia
with a heterogenous pattern12,13. We observed that mela-
noma-associated features aid in distinguishing between
FM and subungual melanoma. The clinical diagnosis should
be supported by dermoscopy findings as it may be benefi-
cial if a biopsy or mycologic examination of the lesions is
required. There are some limitations to this study. Since
differential diagnosis of FM from malignant melanoma is
important in cases of pigmented lesions of the nail units,
especially in melanonychia of the elderly, histopathologic
evaluation is essential for an accurate diagnosis. However,
patients with FM in this study were diagnosed based on
Characteristic Features of Fungal Melanonychia
Vol. 32, No. 6, 2020
465
clinical findings and KOH smear tests only. This study has
a retrospective design and a small number of patients;
therefore, a prospective study with a larger scale is needed.
However, this study is meaningful as it compares not only
general dermoscopic patterns but also each specific der-
moscopic feature between rare FM and subungual mela-
noma, which is the most important discriminating disease.
In conclusion, we suggest that two general dermoscopic
patterns (distal diffuse and linear) and FM-associated spe-
cific dermoscopic patterns can be used as diagnostic clue
to differentiate FM from subungual melanoma. In the fu-
ture, it is necessary to confirm the results through large-
scale follow-up studies.
CONFLICTS OF INTEREST
The authors have nothing to disclose.
FUNDING SOURCE
This work was supported by a 2-year Research Grant of
Pusan National University.
DATA SHARING STATEMENT
The data that support the findings of this study are avail-
able from the corresponding author upon reasonable re-
quest.
ORCID
Hak-Jun Kim, https://orcid.org/0000-0003-1723-4244
Tae-Wook Kim, https://orcid.org/0000-0001-8922-8754
Sung-Min Park, https://orcid.org/0000-0002-4915-8111
Hyun-Joo Lee, https://orcid.org/0000-0002-1088-0975
Gun-Wook Kim, https://orcid.org/0000-0003-1599-7045
Hoon-Soo Kim, https://orcid.org/0000-0002-7649-1446
Byung-Soo Kim, https://orcid.org/0000-0003-0054-8570
Moon-Bum Kim, https://orcid.org/0000-0003-4837-0214
Hyun-Chang Ko, https://orcid.org/0000-0002-3459-5474
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... Dermoscopy can help differentiate onychomycosis from similar conditions including nail psoriasis and traumatic nail dystrophy [3] and can be used to characterize fungal melanonychia [4][5][6][7]. However, the sensitivity and specificity of the dermoscopic signs of onychomycosis are yet to be determined. ...
... Overall, 5 contributions were not in the English language, and 7 did not include information regarding the frequency of dermoscopic signs of onychomycosis. Consequently, 33 records were included in this review [2,3,[12][13][14][15][16][17][18][19][20][21]4,[22][23][24][25][26][27][28][29][30][31]5,[32][33][34][6][7][8][9][10][11]. The process of selecting relevant articles is illustrated in Figure 1 Methods to diagnose onychomycosis were described in 27 of the included papers. ...
... The process of selecting relevant articles is illustrated in Figure 1 Methods to diagnose onychomycosis were described in 27 of the included papers. The diagnosis was based on KOH examination [4,7,11,16,17,23,[27][28][29][30][31][32]35], fungal culture [2,3,5,8,13,16,19,20,24,25,33,34], and/or histologic examination of nail plates [5,8,10,19,20,24]. ...
Article
Full-text available
Introduction: Onychomycosis represents a global burden accounting for about 50% of nail consultations. Several studies have tried to assess the dermoscopic features of onychomycosis. With the multiplication of papers, several "new" dermoscopic signs keep being added leading to some inconsistency in onychoscopic terminology. Objective: This study aimed to summarize the existing literature on the dermoscopic features of onychomycosis and propose a unified onychoscopic terminology. Methods: The literature search was performed using PubMed and Scopus databases up to October 30, 2021 to identify eligible contributions. In total, 33 records (2111 patients) were included. Results: The main dermoscopic signs of onychomycosis are "ruin appearance", "longitudinal striae" and "spikes" on the proximal margin of onycholytic areas, with a specificity of 99.38%, 83.78%, and 85.64% respectively. The "aurora borealis" sign had the highest sensitivity and specificity. Conclusions: The current review provides a framework for issues related to the onychoscopic terminology of onychomycosis and is intended to serve as an aid for students, teachers, and researchers. We proposed a unifying terminology to describe dermoscopic signs of onychomycosis. Dermoscopic signs of onychomycosis show good specificity and are useful in distinguishing nail psoriasis, trauma, and onychomycosis. It helps differentiate fungal melanonychia from nail melanoma, nevi, and melanocytic activation.
... To describe melanonychia patterns, the classifications by the authors from the original papers were also used. However, when reviewing the scientific articles, a reclassification of melanonychias was carried out when there were photos that involved the classifications mentioned by Starace et al. [14] and Kim et al. [15]. ...
Article
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Fungal melanonychia is an uncommon condition, most typically caused by opportunistic melanin-producing pigmented filamentous fungi in the nail plate. In the present study, the clinical characteristics of patients diagnosed with fungal melanonychia were analyzed through a systematic review of cases reported in the literature. The MESH terms used for the search were “melanonychia” AND “fungal” OR “fungi” through four databases: PubMed, SciELO, Google scholar and SCOPUS. After discarding inadequate articles using the exclusion criteria, 33 articles with 133 cases were analyzed, of which 44% were women, 56% were men and the age range was between 9 and 87 years. The majority of cases were reported in Turkey followed by Korea and Italy. Frequent causal agents detected were Trichophyton rubrum as non-dematiaceous in 55% and Neoscytalidium dimidiatum as dematiaceous in 8%. Predisposing factors included nail trauma, migration history, employment and/or outdoor activities. Involvement in a single nail was presented in 45% of the cases, while more than one affected nail was identified in 21%, with a range of 2 to 10 nails. Regarding the clinical classification, 41% evidenced more than one type of melanonychia, 21% corresponded to the longitudinal pattern and 13% was of total diffuse type. Likewise, the usual dermoscopic pattern was multicolor pigmentation. It is concluded that fungal melanonychia is an uncommon variant of onychomycosis and the differential diagnosis is broad, which highlights the complexity of this disease.
... mechanism underlying the effect of the mutation on mucosal and acral pigmentation remains to be elucidated, several lines of evidence suggest that STK11 plays a vital role in melanocyte biology and suppresses melanocyte transformation 3 . Dermoscopy is a useful tool for the diagnosis and management of acral pigmentation 4,5 . Although PRP is considered to be a highly sensitive and specific sign for acral melanoma, it should be noted that PRPs could also occur in non-melanomic conditions as well 6 . ...
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Peutz-Jeghers syndrome (PJS; MIM 175200) is an autosomal dominant multiple-organ cancer syndrome. It is characterized by brown macules distributed in the perioral skin, oral mucosa, hands and feet, and hamartomatous gastrointestinal polyps that can eventually lead to intestinal obstruction, abdominal pain, bleeding, and anemia. Patients with PJS are at a higher risk of ovarian, testicular, breast, lung, and pancreatic cancers. This predisposition is due to the pathogenic variant in serine/threonine kinase 11 (STK11) gene located on chromosome 19p13.3. Here, we present the dermoscopic findings, histopathologic features of acral pigmentation, and DNA sequencing results of the patient with PJS. We also report a successful removal of acral pigmentation using the Q-switched Nd:YAG laser (QSNYL) treatment. Our results suggest that QSNYL therapy could be a treatment option for acral pigmentation in patients with PJS.
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Background Dermoscopy is a non-invasive adjuvant diagnostic tool that allows clinicians to visualize microscopic features of cutaneous disorders. Recent studies have demonstrated that dermoscopy can be used to diagnose onychomycosis. We performed this systematic review to identify the characteristic dermoscopic features of onychomycosis and understand their diagnostic utility.Methods We searched the Medline, Embase, Scopus, and Cochrane databases from conception until May 2021. Studies on the dermoscopic features of onychomycosis were screened. The exclusion criteria were as follows: fewer than 5 cases of onychomycosis, review articles, and studies including onychomycosis cases that were not mycologically verified. Studies on fungal melanonychia were analyzed separately. We adhered to the MOOSE guidelines. Independent data extraction was performed. Data were pooled using a random effects model to account for study heterogeneity. The primary outcome was the diagnostic accuracy of the dermoscopic features of onychomycosis. This was determined by pooling the sensitivity and specificity values of the dermoscopic features identified during the systematic review using the DerSimonian-Laird method. Meta-DiSc version 1.4 and Review Manager 5.4.1 were used to calculate these values.ResultsWe analyzed 19 articles on 1693 cases of onychomycosis and 5 articles on 148 cases of fungal melanonychia. Commonly reported dermoscopic features of onychomycosis were spikes or spiked pattern (509, 30.1%), jagged or spiked edges or jagged edge with spikes (188, 11.1%), jagged proximal edge (175, 10.3%), subungual hyperkeratosis (131, 7.7%), ruins appearance, aspect or pattern (573, 33.8%), and longitudinal striae (929, 54.9%). Commonly reported features of fungal melanonychia included multicolor (101, 68.2%), non-longitudinal homogenous pigmentation (75, 50.7%) and longitudinal white or yellow streaks (52, 31.5%).Conclusion This study highlights the commonly identified dermoscopic features of onychomycosis. Recognizing such characteristic dermoscopic features of onychomycosis can assist clinicians diagnose onychomycosis by the bedside.
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Ungual melanoma is known to be frequently misdiagnosed, and the primary misdiagnosis of ungual melanoma includes onychomycosis. We report a very rare case of onychomycosis concealing ungual melanoma in situ. A 52- year-old male patient presented with a yellow to brown thickened left great toenail that had existed for 10 years. In the front view, Hutchinson's sign which refers periungual extension of brown-black pigmentation from melanonychia was also observed on his hyponychium. First, fungal infection of his toenail was confirmed with positive KOH result. Next, a nail biopsy after nail avulsion was done to assess Breslow depth and to determine surgical margin. And ungual melanoma was diagnosed with immunohistochemical stains. Non-amputative wide local excision with 5 mm surgical margin followed by skin grafting was done Unfortunately in three years ungual melanoma in situ has recurred 2 times and then progressed to invasive malignant melanoma, so he was referred to the Department of plastic surgery for further invasive surgical treatment and regularly monitored to check the recurrence. According to a prior retrospective study, 52% of ungual melanomas were clinically misdiagnosed. Thus, proper diagnosis of ungual melanoma is very important for the patients' better prognosis. It would be important for physicians to examine the nail plate as well as the underneath structures for patients with nail disease including onychomycosis.
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Background Fungal dermatological diseases are significant public health issues. Dermoscopy is a useful bedside assessment tool that helps clinicians diagnose various skin neoplasms and general dermatological diseases. Aim This brief review aims to update clinicians on the dermoscopic features of cutaneous fungal infections such as tinea capitis, tinea corporis, tinea incognito, onychomycosis, and pityrosporum folliculitis. Methods The PubMed database was searched using the terms “dermoscopy” or its synonyms, “tinea capitis”, “tinea corporis”, “tinea incognito”, “onychomycosis” and “pityrosporum folliculitis”. Results The diagnostic value of dermoscopy is well‐recognised in the evaluation of tinea capitis and onychomycosis. There are fewer studies investigating the dermoscopic features of tinea corporis, tinea incognito and pityrosporum folliculitis, but the current data suggest that dermoscopy can aid clinical evaluation of these diseases. Understanding dermoscopic features of cutaneous fungal infection has the potential to increase diagnostic accuracy. Conclusion Dermoscopy in the evaluation of fungal dermatological diseases has the potential to optimize diagnostic accuracy, reduce unnecessary testing, and, consequently, improve clinical practice.
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Nail unit melanoma (NUM) is a variant of acral lentiginous melanoma. The differential diagnosis is wide but an acquired brown streak in the nail of a fair-skinned adult person must be considered a potential melanoma. Dermoscopy helps clinicians to more accurately decide if a nail apparatus biopsy is necessary. Detailed evaluation of clinical and dermoscopy features and description of conservative surgery of in situ NUM. Retrospective study of in situ NUM diagnosed and treated with conservative surgical management in the authors' center from 2008 to 2013. Six cases of NUM were identified: 2 male and 4 female patients, age range at diagnosis of 44 to 76 years. All patients underwent complete nail unit removal with at least 6-mm security margins around the anatomic boundaries of the nail. The follow-up varies from 4 to 62 months. Nail unit melanomas pose a difficult diagnostic and therapeutic challenge. Wide excision is sufficient, whereas phalanx amputation is unnecessary and associated with significant morbidity for patients with in situ or early invasive melanoma. Full-thickness skin grafting or second-intention healing after total nail unit excision is a simple procedure providing a good functional and cosmetic outcome.
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Background: Diagnosing fungal melanonychia (FM) is often difficult because it mimics melanonychia caused by other factors. Dermoscopy is helpful in the setting of nail pigmentation. However, the diagnostic characteristics of FM on dermoscopy are not fully elucidated. Objective: We sought to determine the dermoscopic characteristics of FM. Methods: We evaluated the dermoscopic patterns of FM diagnosed at 2 university hospitals from January 2010 to February 2016. We included nail matrix melanocytic activation, nail matrix nevi, and nail unit malignant melanomas as control groups for comparison. Results: In all, 18 FM, 24 melanocytic activation of the nail matrix, 27 nail matrix nevi, and 11 malignant melanoma cases were analyzed. Statistical analysis revealed that yellow color, multicolor pattern, nonlongitudinal homogenous pattern, reverse triangular pattern, subungual keratosis, white or yellow streaks, and scales on the nail were more frequent in FM. However, gray color, longitudinal pattern, and pseudo-Hutchinson sign were less frequent in FM than in controls. Limitations: This was a retrospective study from 2 university hospitals, with a small sample size. Conclusion: The results revealed distinctive dermoscopic patterns for FM. Therefore, dermoscopy can be a useful ancillary tool for diagnosing FM.
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Background: Melanonychia may be the presenting sign of ungual melanoma. However, there are insufficient basic clinical data for melanonychia in Korean patients. Objective: We sought to identify basic clinical data and devise a classification algorithm for melanonychia. Methods: In all, 275 patients with melanonychia who visited our clinic from January 2002 to August 2014 were included in this study. We reviewed medical records, clinical and dermoscopic photographs, and histopathologic findings and we assessed demographics (eg, age); medical (eg, systemic diseases), family, and trauma (eg, nail biting) history; and physical findings (eg, affected number and site). Results: The 5 most common causes of melanonychia in Korean patients were subungual hemorrhage (29.1%), nail matrix nevus (21.8%), trauma-induced pigmentation (14.5%), nail apparatus lentigo (11.6%), and ethnic-type nail pigmentation (8.0%). Melanoma was diagnosed in 6.2% of patients. Ethnic-type nail pigmentation was commonly identified. Limitations: This is a retrospective study from a single center. Conclusion: We propose a revised diagnostic algorithm for melanonychia to assist in the evaluation of this condition.
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Background: Modern antifungal drugs achieve high cure rates in onychomycosis of the toes, but little is known about the long-term evolution of the treated patients. Objective: We evaluated the compliance and long-term follow up of onychomycosis after treating the 438 patients with one of the 3 drugs including itraconazole, terbinafine and fluconazole. Methods: On the basis of the patients' charts, photographs and telephone visiting, we investigated the positivity of the diagnostic methods, compliance and long-term follow up results of the onychomycosis treated with one of the three drugs including itraconazole, terbinafine and fluconazole from January 1999 to August 2002 in the Department of Dermatology, St. Mary's hospital, the Catholic University of Korea, Seoul. Results: 1. The positivity rates of the KOH smear, fungus culture and KONCPA test were 68% (283/418), 18% (65/354) and 89% (178/200), respectively. 2. The percentage of the patients who had completely finished the course of the treatment were 61% (191/315) in the itraconazole-treated, 43% (30/69) in the terbinafine-treated and 21% (3/14) in the fluconazole-treated. 3. Cure rates after 1 year of the treatment were 34% (56/167) in the itraconazole-treated, 29% (10/35) in the terbinafine-treated and 86% (6/7) in the fluconazole-treated. Cure rate after 2 years of the treatment were 33% (17/51) in the itraconazole-treated, 8% (1/12) in the terbinafine-treated. Cure rates after 3 years of the treatment were 29% (9/31) in the itraconazole-treated, 10% (1/10) in the terbinafine-treated. 4. Cure rates after more than 1 year of the treatment were 33% (82/249) in the itraconazole-treated, 21% (12/57) in the terbinafine-treated. 5. Cure rates of the completely treated groups were 36%, 37% and 40% after 1 year, 2 years and 3 years in the itraconazole-treated and 44%, 20% and 20% after 1 year, 2 years and 3 years in the terbinafine-treated. Conclusion: In the treatment of onychomycosis, compliance rate varied very much according to the duration or method of medication, but the cure rates are different after more than 2 years of follow up between the itraconazole-treated and the terbinafine-treated.
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Background: Although there have been many studies about tinea unguium, few studies about etiologic agents including nondermatophytic molds and yeasts in onychomycosis have been reported in Korea. Objective: The purpose of the study was to investigate the recent clinical features and identification of etiologic agents in onychomycosis. Methods: In the 3-year period 1999-2002, we reviewed five hundred ninty nine patients with onychomycosis in retrospectively. The etiologic agents were identified by cultures on Sabouraud's dextrose agar with and without cycloheximide. The identification of yeasts based on the results of culture, germ tube test, and biochemical API system tests. Nondermatophytic molds or yeasts isolated were considered as pathogens when the presence of fungal elements was identified at direct microscopy and follow-up specimen yielding cultures showed the same fungi. Results: Of the five hundred ninty nine patients presenting with onychomycosis, 92.5% were toenail onychomycosis, 5.5% fingernail onychomycosis, and 2.0% onychomycosis in both toenails and fingernails. Among the age groups, the incidence rate was highest in the fifth decade(22.0%). The ratio of male to female patients was 1.1:1. Distal subungual onychomycosis(96.1%) was the most common clinical type of onychomycosis. In the toenail onychomycosis, dermatophytes were most frequently isolated(81.9%), followed by yeasts(11.7%), and nondermatophytic molds(6.4%). Trichophyton rubrum was the most frequently isolated agent. In the fingernail onychomycosis, yeasts were mostly isolated(48.2%), followed by dermatophytes(44.4%), and nondermatophytic molds(7.4%). Conclusion: Because of the increase in onychomycosis by nondermatophytic molds and yeasts, we suggest the need of a careful mycological examination in patients with onychomycosis.
Article
Background: Although there have been many studies about onychomycosis, no study about Koreans in onychomycosis has been reported in Korea. Objective: The purpose of this study was to investigate the onychomycosis in Koreans. Methods: From April, 2009, to March, 2010, 1,893 patients with onychomycosis who visited the department of dermatology at 10 university hospitals were evaluated. Results: Of 1,893 patients with onychomycosis, 93.8% were toenail onychomycosis, 2.2% fingernail onychomycosis, and 4.0% onychomycosis in both toenails and fingernails. Among the age groups, the incidence rate was highest over the sixties (35.6%). The ratio of male to female patients was 1.3:1. Distal and lateral subungual onychomycosis (80.3%) was the most common clinical type of onychomycosis. Combination therapy of oral terbinafine or itraconazole and topical amorolfine nail lacquer was most common in the treatment of onychomycosis. The most common reasons for combination therapy in onychomycosis were higher cure rate due to synergistic activity (40.2%), followed by shortened treatment duration (12.8%), patient compliance (12.3%), and prevention of recurrence and reinfection (1.7%). Conclusion: Because of the increase in onychomycosis, we suggest the need of standard treatment guidelines for Korean patients with onychomycosis.
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Background: Onychopapilloma is a benign neoplasm of the nail bed and the distal matrix. Although not uncommon in our experience, only up to 32 cases of this tumor have been reported in the literature. Objective: We sought to review the clinical, dermoscopic, and pathologic features of onychopapilloma. Methods: We retrospectively analyzed the clinical features of 47 patients with pathologically confirmed onychopapilloma diagnosed within the last 5 years, and reviewed the published literature. Results: The most common clinical presentation was longitudinal erythronychia (n = 25); followed by longitudinal leukonychia (n = 7); longitudinal melanonychia (n = 4); long splinter hemorrhages without erythronychia, leukonychia, or melanonychia (n = 8); and short splinter hemorrhages without erythronychia, leukonychia, or melanonychia (n = 3), with subungual mass (n = 47) and distal fissuring (n = 11). Pathology was consistent with acanthosis of the nail bed and distal matrix, with matrix metaplasia underlying distal subungual hyperkeratosis. Limitations: This was a retrospective analysis. Conclusion: To our knowledge, our series of onychopapilloma is the largest so far. Among various clinical presentations, longitudinal erythronychia is the most common. Dermoscopy of the free edge of the nail plate showing a small subungual keratotic mass where the band reaches the nail plate margin provides a clue for the diagnosis.
Article
Data on the dermoscopic features of fungal melanonychia are limited. To identify the dermoscopic features of fungal melanonychia. We reviewed patient files, clinical history and dermoscopic images of all cases with a diagnosis of fungal melanonychia seen at our dermoscopy unit within the past year. In total, 14 cases with 20 involved nails were reviewed. The most common type of melanonychia was melanonychia striata (7/20). Multicoloured pigmentation was observed in 19 of the nails. The main dermoscopic pattern was homogeneous pigmentation; however, black pigmented aggregates, presenting as either coarse granules or pigmented clumps, accompanied this homogeneous pigmentation in 16 lesions. Matt black pigmentation, matt white pigmentation, yellow to brown pigmentation, black reverse triangle (wider at the distal than the proximal end), superficial transverse striation and blurred appearance were the other features. We have identified a number of dermoscopic features appearing in fungal melanonychia, which should help in diagnosis of this disease. © 2014 British Association of Dermatologists.
Article
Background Subungual haemorrhages are characterized by well-circumscribed dots or blotches with a red to red–black pigmentation, but some cases can be difficult to distinguish from subungual melanoma by the naked eye alone. Dermoscopy has proven to be a useful, noninvasive tool in the diagnosis of pigmented lesions in the nail; however, few dermoscopic studies of subungual haemorrhages have been reported. Objectives To investigate characteristic dermoscopic patterns of subungual haemorrhages, and to find distinctive features that can differentiate them from nail-unit melanomas. Methods Patients with a confirmed diagnosis of either subungual haemorrhage or nail-unit melanoma at a tertiary university hospital were included in the study. Clinical features and dermoscopic patterns were evaluated. Results Sixty-four patients with a total of 90 lesions of subungual haemorrhage were enrolled in the study. The majority of cases (84%) showed combinations of more than one colour, while 16% had only one colour. The most common colour of the subungual haemorrhages was purple–black, in 37% of cases. A homogeneous pattern was observed in 92% of cases, globular patterns in 42% and streaks in 39%. Peripheral fading and periungual haemorrhages were found in 54% and 22% of cases, respectively. Destruction or dystrophy of the nail plate was observed in 16% of cases. In the 16 cases of nail-unit melanomas, Hutchinson sign, longitudinal irregular bands or lines, triangular shape of bands, vascular pattern, and ulcerations were found in 100%, 81%, 25%, 6% and 81% of cases, respectively. In contrast, these features were not found in subungual haemorrhages. Conclusions Dermoscopy provides valuable information for the diagnosis of subungual haemorrhage and aids in the differential diagnosis from nail-unit melanoma.
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Nail dermoscopy is becoming more and more frequently utilized for the diagnosis of nail disorders. It can be performed with handy dermoscope or with a video dermoscope, which allows magnifications of up to 200. Nail dermoscopy requires a good knowledge of nail anatomy and physiology and the pathogenesis of nail diseases: we have to know which part of the nail we have to look at! The nail is in fact not visible as a whole at one time, but its different parts should be observed, moving the lens back and forth and transversally. All nail disorders can be observed by dermoscopy. However, except for some diseases in which the technique really adds a lot to clinical examination, in most of the cases, nail dermoscopy only permits a better visualization of symptoms already evident to the naked eye. Dermoscopic features of nail signs are always very interesting and surprising, and may help in our understanding of nails.