ArticlePDF Available
International Journal of
Respiratory and Pulmonary Medicine
Mathur et al. Int J Respir Pulm Med 2017, 4:069
Volume 4 | Issue 2
DOI: 10.23937/2378-3516/1410069
Page 1 of 3
ISSN: 2378-3516
Open Access
Citaon: Mathur P, Namana V, Gupta SS, Berger B, Bondi E (2017) Pleural Lipoma. Int J Respir Pulm
Med 4:069. doi.org/10.23937/2378-3516/1410069
Received: December 14, 2016; Accepted: April 10, 2017; Published: April 13, 2017
Copyright: © 2017 Mathur P, et al. This is an open-access arcle distributed under the terms of the
Creave Commons Aribuon License, which permits unrestricted use, distribuon, and reproducon
in any medium, provided the original author and source are credited
Mathur et al. Int J Respir Pulm Med 2017, 4:069
Pleural Lipoma
Pankaj Mathur1, Vinod Namana2*, Sushilkumar S Gupta2, Barbara Berger3 and Ellio Bondi4
1Department of Medicine, University of Arkansas for Medical Sciences, USA
2Department of Medicine and Cardiology, Maimonides Medical Center, USA
3Department of Medicine, Wyco Heights Medical Center, USA
4Department of Pulmonary and Crical Care, Brookdale University Medical Center, USA
*Corresponding author: Vinod Namana, MD, MPH, Department of Cardiology, Fellow in Cardiovascular Medicine, 4802
10th Avenue, Brooklyn, NY 11219, USA, Tel: +718-283-6892, E-mail: vnamana@maimonidesmed.org
Keywords
Lipoma, Pleural lipoma, Liposarcoma, Fibroma
skin and subcutaneous ssue; occurring with an annual
incidence of 1 per 1000 persons [1]. Lipomas are histolog-
ically made up of abundant mature adipose ssue with no
mitoc acvity. Lipomas are uncommonly found in viscer-
al locaons such as stomach, kidney, brain, especially in
the corpus callosum, and thoracic cavity [1,2]. Intrathoracic
lipomas were rst described by Fothergill in 1781 [3]. Clin-
ically pleural lipomas and other intrathoracic lipomas are
slow growing benign tumors, oen diagnosed coinciden-
tally. Somemes they may grow to a large size and cause
compression symptoms such as dyspnea and dysphagia.
CLINICAL IMAGE
Case Descripon
A 31-year-old male presented with complaints
of a mild non-producve cough for 2 months. He had no
history of smoking, fever, chills, rigors, weight loss, dys-
pnea, chest pain and hemoptysis. There was no histo-
ry of exposure to occupaonal hazards or medicaons
use. He was hemodynamically stable and had no signi-
cant ndings on physical examinaon. Postero-anterior
radiography of the chest showed a pleural-based mass
in the right upper lung eld (Figure 1). Computed to-
mography (CT) of the chest was suggesve of a smooth,
marginated mass in the right upper thorax, measuring
5.4 × 4.5 × 2.7 cms (Figure 2). The mass contained fat
and so-ssue density with no calcicaons; there were
no bony erosions. Fat planes between right intercostal
muscles and pectoralis muscle were intact. CT-guided
biopsy was performed and histopathology conrmed the
diagnosis of pleural lipoma. The ssue consisted of ma-
ture adipose cells (Figure 3). The eology of cough was
not aributed to the pleural lipoma; neither there were
any signs of bacterial infecons. He was inially treated
with antussive dextromethorphan syrup, followed by
inhaled corcosteroids which led to complete recovery
from the symptom.
Discussion
Lipomas are the most common benign tumors of the
Figure 1: Postero-anterior radiography of the chest showing
a pleural-based mass in the right upper lung eld (red arrow).
ISSN: 2378-3516DOI: 10.23937/2378-3516/1410069
Page 2 of 3
Mathur et al. Int J Respir Pulm Med 2017, 4:069
racoscopic surgery (VATS). The proponents of early surgi-
cal intervenon suggest that surgical procedure is easi-
er if performed earlier as there are less neighboring adhe-
sions and ssue inltraon. Besides, these tumors have
a variable growing rate and may cause compression of the
lung parenchyma and intra parenchymal bleeding [14]. In the
studies of Sakurai, et al. [2] 8 out of 10 paents were asymp-
tomac and in Jayle, et al. [14] 4 out of 5 paents were as-
ymptomac. The CT scan guided biopsy was performed in
only 1 paent by Sakurai, et al. [2] and in 2 paents by Jayle,
et al. [14]. In our case, we found that CT scan guided biop-
sy was clearly benecial as it diagnosed the benign nature of
the tumor, besides in paents undergoing surgical resecon
there is always a chance of local recurrence albeit small <
5% [2] and incomplete removal leading to the complicated
surgical procedure [2,14]. Therefore for an asymptomac
paent, we think before going for more invasive procedures
like postero-lateral thoracotomy or VATS, CT scan guided bi-
opsy should be considered. However, for large size tumors,
surgical resecon or video-assisted thoracoscopic surgery
(VATS) is preferred to prevent compressive symptoms [2].
All the opons were discussed with our paent in
detail and he chose conservave management, due to
the absence of clinical signs and symptoms secondary
to pleural lipoma, the low risk prole for malignancy,
availability of the conrmed diagnosis, and he also did
not want to take the unnecessary risk of surgery.
References
1. Rydholm A, Berg NO (1983) Size, site and clinical incidence
of lipoma. Factors in the differential diagnosis of lipoma and
sarcoma. Acta Orthop Scand 54: 929-934.
2. Sakurai H, Kaji M, Yamazaki K, Suemasu K (2008) Intratho-
racic lipomas: their clinicopathological behaviors are not as
straightforward as expected. Ann Thorac Surg 86: 261-265.
3. Fothergill J Medical and Philosophical Works. John Walker
Printer, London, 1781: 508-528.
4. Rao N, Dworecka F, Hermann G (1982) Cervical radiculopa-
Importantly, they have also been associated with compli-
caons such as cervical radiculopathy [4], rib fracture [5],
pneumonia and empyema [6].
Invesgaons
CT of the chest is the inial invesgaon of choice, but
biopsy of the tumor remains the gold standard. The dier-
enal diagnosis includes liposarcomas, bromas and soli-
tary brous tumor of the pleura (SFTP). Benign lipomas are
usually smooth, marginated, have uniform fay density, lo-
cated peripherally in the chest wall and usually on CT scan
have aenuaon coecients of -50 to -150 Hounseld
units [7], whereas Liposarcomas can be present anywhere
in the thoracic cavity, but more frequently are found in
the posterior mediasnum. Lipo sarcomas have aenu-
aon coecients of higher than -50 Hounseld units [7].
Histologically, pleural and intrathoracic lipomas contain
abundant mature adipose ssue with no mitoc acvity,
with normal bro-connecve ssue in between but some-
mes may contain foci of calcicaon and fat necrosis es-
pecially in large tumors [8]. Lipo sarcomas, on the other
hand, have adipose Cells of varying size with hyperchro-
mac nuclei and eosinophilic cytoplasm. Liposarcomas can
also have mitoses associated with mulnucleated hiso-
cytes and fay necrosis seen in 25% of cases [8,9]. SFTP
is a rare, usually benign and indolent growing tumor that
accounts for approximately 5% of all pleural neoplasms
[10]. More than 50% of benign tumors are asymptomat-
ic, and are incidentally discovered on roune chest x-rays
performed for paent presenng with cough, chest pain or
dyspnea [11]. Histologically they consist of ovoid or elon-
gated spindle-shaped tumor cells with varying amounts of
cytoplasm [12].
Management
Epler, et al. suggested, pleural lipomas can be man-
aged conservavely and should be followed radiological-
ly [7]. However, recently several authors such as Sakurai,
et al. [2], Chung, et al. [13], and Jayle, et al. [14] advocated re-
secon of the lipoma tumor by surgery or video-assisted tho-
[R] [L]
Figure 2: Computed tomography of the chest showing CT-
guided biopsy of a smooth, marginated mass in the right upper
thorax, measuring 5.4 × 4.5 × 2.7 cms.
Figure 3: Histology shows normal mature adipose tissue, with
no mitotic activity.
ISSN: 2378-3516DOI: 10.23937/2378-3516/1410069
Page 3 of 3
Mathur et al. Int J Respir Pulm Med 2017, 4:069
10. Lee CE, Zanariah H, Masni M, Pau KK (2010) Solitary brous
tumour of the pleura presenting with refractory non-insulin me-
diated hypoglycaemia (the Doege-Potter syndrome). Med J
Malaysia 65: 72-74.
11. Campbell NA, Antippa PN (2006) Solitary brous tumour of
the pleura. Heart Lung Circ 15: 400-401.
12. Robinson LA (2006) Solitary brous tumor of the pleura. Can-
cer Control 13: 264-269.
13. Chung JH, Moon DS, Oh HE, Park CS, Choi JE (2005) A
case of pleural lipoma treated with video assisted thoracic
surgery (VATS) Tuberc Respir Dis 59: 556-560.
14. Jayle C, Hajj-Chahine J, Allain G, Milin S, Soubiron L, et al.
(2012) Pleural lipoma: a non-surgical lesion? Interact Car-
diovasc Thorac Surg 14: 735-738.
thy caused by lipoma. Patient with multiple congenital skel-
etal anomalies and intraspinal and intrathoracic lipomas. N
Y State J Med 82: 222-225.
5. Buxton RC, Tan CS, Khine NM, Cuasay NS, Shor MJ, et al.
(1988) Atypical transmural thoracic lipoma: CT diagnosis. J
Comput Assist Tomogr 12: 196-198.
6. Ouadnouni Y, Bouchikh M, Bekarsabein S, Achir A, Smahi
M, et al. (2009) Endobronchial lipoma a rare cause of pleu-
ral empyema: a case report. Cases J 2: 6377.
7. Epler GR, McLoud TC, Munn CS, Colby TV (1986) Pleural li-
poma. Diagnosis by computed tomography. Chest 90: 265-268.
8. Hagmaier RM, Nelson GA, Daniels LJ, Riker AI (2008) Suc-
cessful removal of a giant intrathoracic lipoma: a case re-
port and review of the literature. Cases J 1: 87.
9. Weiss SW, Enzinger FM, Goldblum JR (1994) Histological Typ-
ing of Soft Tissue Tumours. Lipomatous Tumours 23-26.
Article
Full-text available
Introduction and importance Lipoma is a benign tumor that arises from adipose tissue; subcutaneous fat is the most common site. It is the most common soft tissue tumor in adulthood. They are usually curable with simple excision. They are slow growing and can rarely become cancerous. Lipomatosis is when there are multiple lipomas with different pedicles. Lipomas arising from the thoracic pleura are rare and intrathoracic lipomatosis is exceptionally rare. Here we report a case of huge lipomatosis removed from the right pleural cavity in a 65 years old man. Case presentation A 65 years old male from southern region of Ethiopia, presented with shortness of breath associated with chest pain, productive cough, easy fatigability, and dyspnea on exertion. On exams, he had dullness on chest percussion and absent air entry on the right hemichest on auscultation. He had a history of treatment for pulmonary tuberculosis seven years back. Chest CT showed huge lobulated heterogeneous mass in the right pleural space with significant mediastinal shift to the left. All the large and small masses were removed by a thoracotomy and the specimen was subjected to histopathology examination which revealed myxoid lipoma. Discussion Lipoma is a benign tumor with no risk of malignant transformation. Intrathoracic lipoma is quite rare that we don't really find much reported cases. Conclusion Intrathoracic lipomatosis is a rare condition that progresses without symptoms until it reaches a big size, at which point compressive symptoms appear. The primary approach for both diagnostic and therapeutic purposes continues to be surgical resection.
Article
Full-text available
Until recently, a definitive diagnosis of lipoma in the thorax could only be established by thoracotomy. We undertook this study to determine if chest CT could provide such an answer. Among 4,000 chest CT scans, six patients were found to have lipoma according to the following selected criteria: CT features of a pleural mass; a lesion showing completely homogeneous density with CT numbers indicating fat, and exclusion of other fatty lesions. In these six patients, the lipoma was an incidental finding, four were men, the mean age was 64.3 years, one-half were obese, and none had chest pains or dyspnea. Lesions varied in size from 2 to 4 cm and occurred along the chest wall. The CT numbers of the masses ranged from -54 to -129. None developed malignancy. In conclusion, we recommend clinical and chest CT follow-up for the asymptomatic patient who fulfills our CT criteria for lipoma. Biopsy or resection is recommended for lesions that are inhomogeneous.
Article
Full-text available
We report a case of a 61 year-old man who presented with refractory non-insulin mediated hypoglycaemia. A chest radiograph showed a right lung opacity, which was confirmed as a large intra-thoracic mass by computed tomography (CT) of the thorax. CT-guided biopsy with histological examination revealed features of a solitary fibrous tumour of low malignant potential. We discuss the association of solitary fibrous tumour of the pleura (SFTP) with hypoglycaemia, and the management of such rare tumours.
Article
Full-text available
Benign neoplasm of the endobronchial tree is quite rare, while endobronchial lipoma is extremely rare. The irreversible pulmonary damage is due to progressive bronchial obstruction; even so, pleural empyema is exceptionally encountered in a case of endobronchial lipoma. We report a case of a 47-year-old man who had left lung pneumonia with hemoptysis. The chest computed tomography showed cystic bronchiectasis with pleural effusion, Flexible bronchoscopy revealed a round tumor on the left main bronchus.
Article
Full-text available
We report a case of a 44-year old female who presented to her physician complaining of mild dyspnea. A follow-up chest X-ray and chest computed tomography scan revealed a giant bilateral intrathoracic mass, filling the right thoracic cavity and extending across the anterior mediastinum into the left chest cavity. This large mass caused a marked shift in the midline structures, displacing the heart to the left hemi-thorax. The patient underwent surgical removal of the thoracic and breast mass, with histologic examination confirming the diagnosis of a giant intrathoracic lipoma, weighing 4,320 grams and measured 34 x 28 x 11 cm. It is the largest intrathoracic lipoma documented in the modern literature.
Article
Pleural lipomas are benign tumours that develop at the expense of adipose tissues, and they never evolve towards liposarcoma. Located usually at the mediastinal, bronchial and pulmonary levels, a pleural situation is extremely rare. Chest X-rays usually detect them and computed tomography scans confirm the diagnosis. As complications occur, a wait-and-see policy is common. We report our pleural lipoma surgical exeresis experience since 1999. We have operated on five cases of pleural lipomas among nearly 1800 cases of thoracic exeresis: three male and two female patients, without obesity (in all cases, body mass index (BMI) < 28). The mean age was 54.6 years (range 35–72 years). Four patients were electively operated and one in emergency, three with video-assisted thoracic surgery (VATS) procedure and two with open chest surgery, without recurrent cases. Advancements in VATS have greatly reduced the morbidity rate of these benign tumours especially if exeresis is performed early on a small, uncomplicated adhesion-free tumour. On the other hand, the operation may be deleterious, complicated by the presence of a large lipoma or in a complicating situation. In our opinion, we should revise the wait-and-see policy when facing these lesions considering their evolutionary potential. We should advise VATS in pleural lipomas.
Article
Two cases of transmural thoracic lipomas demonstrate a pattern of rib involvement that has not been previously reported. The lipomas presented with an otherwise characteristic appearance on plain radiography and CT.
Article
All 428 patients who had a non-visceral lipoma histopathologically diagnosed during 1 year in a defined population (0.74 million inhabitants) were analysed retrospectively as regards the age, duration of symptoms, size, site (location and depth) and multiplicity of the lipomas. Solitary subcutaneous lipomas were uncommon in the hand, thigh, lower leg and foot, and four-fifths of them (264/338) were smaller than 5 cm. Multiple subcutaneous lipomas were found in 61 patients, most of them young males. Subfascial lipomas, with a mean size (6 cm) double that of solitary subcutaneous lipomas, were found in 13 patients. A subgroup of 192 lipomas (153 patients) was reexamined histologically and the tumours were classified as either simple lipoma or angiolipoma. Angiolipomas were significantly more common in patients with multiple lipomas. To assess the reliability of a clinical diagnosis of lipoma as well as the proportion of clinically diagnosed lipomas not verified by histology, the records of patients seen in one department of surgery and in one health care centre were examined. Based on these data, the annual clinical incidence of lipoma (number of patients consulting a doctor for a lipoma, even if not histologically verified) was estimated to be 1/1000. When the data for solitary lipomas were compared to those for soft-tissue sarcoma, it was found that patient age and duration of symptoms were of minor value in the clinical differential diagnosis. However, if a tumour were (a) larger than 5 cm, irrespective of depth and location, (b) located in the thigh, irrespective of depth and size, or (c) deep, irrespective of location and size, it was more likely to be a sarcoma. These findings can be used in selecting patients for referral to a tumour centre before surgery.
Article
Solitary fibrous tumours of the pleura are rare tumours originating from the mesenchymal cells of the submesothelial tissue of the pleura. The tumours may present in a variety of ways, ranging from no symptoms, to local symptoms such as dyspnoea, cough and chest pain, through to systemic symptoms such as clubbing and hypoglycaemia. We present a case of a solitary fibrous tumour, which presented with clubbing. © 2006 Australasian Society of Cardiac and Thoracic Surgeons and the Cardiac Society of Australia and New Zealand.