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19. NCI-Loeffler’s syndrome +

Authors:
Oner Ozdemir
Division of Allergy and Immunology, Department of Pediatrics, Sakarya University Training Research and Hospital, Sakarya, Turkey
North Clin Istanb
doi: 10.14744/nci.2020.40121
Loefer’s syndrome: A type of eosinophilic pneumonia
mimicking community-acquired pneumonia and
asthma that arises from Ascaris lumbricoides in a child
Here, we describe a patient with Loeffler’s syndrome
initiated by Ascaris lumbricoides, who mimicked
the clinical picture of community-acquired pneumonia
(CAP) and bronchial asthma. A 5-year-old male child
was presented to an outside center with complaints of
cough, dyspnea, wheezing, intermittent fever for three
days. He was diagnosed with pneumonia after physical
and radiological evaluations then admitted for treatment
at an outside hospital. After discharge, his symptoms
decreased but persisted for several weeks and coughed
a substance up by sputum expectoration (Fig. 1). When
he presented to us, he seemed to be in a good general
condition, but his physical exam revealed coarse poly-
phonic rhonchi, especially on the upper zone of the left
lung. Evaluation of the peripheral blood smear of the pa-
tient demonstrated mounting eosinophilia (from 0.2% to
2.06%–338/mm3-), while IgE was 50 IU/mL. A chest
X-ray demonstrated unilateral upper zone patchy con-
solidation (pneumonic infiltrations) of the left lung (Fig.
2A). Despite antibiotic therapy, consolidation was not
resolved but almost completely vanished when he vom-
ited the parasite up (Fig. 2B). Macroscopic evaluation of
Original Images ALLERGY & IMMUNOLOGY
Cite this article as: Ozdemir O. Loefer’s syndrome: A type of eosinophilic pneumonia mimicking community-acquired pneumonia and
asthma that arises from Ascaris lumbricoides in a child. North Clin Istanb
UNCORRECTED PROOF
Received:
January 20, 2020
Accepted:
January 14, 2020
Online:
August 05, 2020
Correspondence: Oner OZDEMIR, MD. Sakarya Universitesi Egitim ve Arastirma Hastanesi, Cocuk Sagligi ve Hastaliklari
Anabilim Dali, Alerji ve Immunoloji Bilim Dali, Adapazari, Sakarya, Turkey.
Tel: +90 264 444 54 00 e-mail: ozdemir_oner@hotmail.com
© Copyright 2020 by Istanbul Provincial Directorate of Health - Available online at www.northclinist.com
Figure 1. The most common intestinal parasite (worm, As-
caris) in humans is seen after coughed up by the patient.
Figure 2. Pneumonia caused by the nematode Ascaris lum-
bricoides. Extraintestinal manifestations of ascariasis such
as pulmonary ascariasis, “Loefer’s syndrome”, are not com-
mon and can be misdiagnosed. Pneumonic inltration at the
upper lobe of the left lung (A) is shown. The appearance of
left lung (B) is seen after the patient coughed the worm up.
A B
North Clin Istanb
2
the substance was confirmed as Ascaris lumbricoides by
microbiologists.
e patient was diagnosed with Loeffler’s syn-
drome, in which eosinophils gather in the pulmonary
tissue in regards to a parasitic infection. Loeffler’s syn-
drome should be thought early in the differential diag-
nosis for CAP and asthma, which is unresponsive to
classic antibiotic therapy in individuals if they live in
an endemic region for parasitic diseases in the devel-
oping countries [1, 2].
Informed Consent: Informed consent was obtained orally from
the patient’s father who participated in this report.
REFERENCES
1. Acar A, Oncül O, Cavuşlu S, Okutan O, Kartaloğlu Z. Case report:
Löffler’s syndrome due to Ascaris lumbricoides mimicking acute
bacterial community-acquired pneumonia. Turkiye Parazitol Derg
2009;33:239–41.
2. Deveci U, Üstün C, Altınsoy HB, Akay A, Özdiller S, Aydın M. Loef-
fler’s syndrome mimicking bronchial asthma and pneumonia in a child:
case report. Turkiye Parazitol Derg 2013;37:288–91.
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Article
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A 14-year-old male child was hospitalized with complaints of a bronchial wheezing, cough, dyspnea, and sputum and a preliminary diagnosis of bronchial asthma and pneumonia. The patient was treated empirically for bronchial asthma and pneumonia, but gave neitherr clinical nor radiological response to treatment. On the high-resolution computerized tomography, a typical spiral image of Ascaris lumbricoides was identified inside a cavity in the upper lobe of the left lung with a diameter of 8x7 cm. Also,migratory pneumonic infiltrations progressing between the lower lobe and hilary region of the left lung were seen. Examination of the peripheral blood smear of the patient revealed eosinophilia (40%), while IgE was measured as 350 IU/mL. The patient was diagnosed as "Loeffler's syndrome" due to A. lumbricoides", and successfully treated with mebendazole 2x100 mg/day for three days. Loeffler's pneumonia should be considered when patients with bronchial asthma and pneumonia do not respond to specific treatment in developing countries. Radiological investigations may be available in the diagnosis of parasitic infections. In this case, early diagnosis by radiologic methods have prevented unnecessary drug use and related complications. (Turkiye Parazitol Derg 2013; 37: 288-91).
Article
Full-text available
In this study we present a patient with Loeffler's syndrome caused by Ascaris lumbricoides who presented with the clinical findings of community-acquired pneumonia (CAP). Our patient, who was twenty-five years old, and who had had symptoms such as coughing, expectorating, dyspnea and fever for approximately ten days, was hospitalized. We auscultated polyphonic rhonchuses at the both hemithoraxes. A chest X-ray revealed bilateral lower zone patch consolidation. Acute bacterial community acquired pneumonia (CAP) was diagnosed due to these findings and empirical antibiotic treatment was begun. Repeated sputum Gram stains were negative, and both sputum and blood cultures were sterile. A sputum smear was negative for acid-fast bacilli. The patient's fever and respiratory complaint did not respond to the empirical antibiotics therapy. During the course of advanced investigations, we measured peripheric eosinophilia, and high levels of total Eo and total IgE, and observed Ascaris lumbricoides eggs during stool examination. The patient was given a diagnosis of Loeffler's syndrome. Thereupon the patient was treated successfully with one dose of albendazol 400 mg. In conclusion, we suggest that Loeffler's syndrome must be considered early in the differential diagnosis for CAP when peripheric eosinophilia is seen in patients if they live in an endemic area for parasitic disease.