Langerhans cell histiocytosis mimicking acute otitis media in childhood—a case presentation

نویسندگان

چکیده

Abstract Background Langerhans cell histiocytosis (LCH) is an abnormal polyclonal proliferation of cells that affect different parts the body. Temporal bone involvement quite common among involved sites. The etiology unknown. Diagnosis based on symptoms, imaging, and histopathology. Especially LCH in temporal confused with acute or subacute otitis media. There are many treatment options LCH. Case presentation Here, a 2-year-old pediatric patient pain right ear was diagnosed as having result examinations. MRG revealed multiple lesions bone, sphenoid clivus. She treated steroids vinblastine. Conclusion Possible tumoral formations should be kept mind when children complain otalgia media-like clinical picture for long time.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Langerhans cell histiocytosis

Introduction: Langerhans cell histiocytosis (LCH), which was previously known as histiocytosis X, refers to a group of lesions that stimulate uncontrolled proliferation of cells. The purpose of this case was to report and describe a LCH case with mandibular bone involvement in a 2.5-year-old boy. Case reports: A 2.5 years old boy with LCH of mandibular jaw who has been treated by surgical inter...

متن کامل

Current Treatment Strategy in Langerhans Cell Histiocytosis

Langerhans cell histiocytosis (LCH) is a rare disorder described as three different entities including eosinophilic granulomaof bone, the Hand-Schuller-Christian syndrome, and Letterer-Siwe disease. LCH is currently classified into singlesystem LCH, and multisystem LCH. Patients with single system LCH have an excellent prognosis, and are mostlytreated with local therapy. Multisystem LCH is subd...

متن کامل

A Case of Langerhans Cell Histiocytosis with Atypical Radiological Presentation.

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial lung disease characterized by the accumulation of histiocytes within the airspaces or parenchyma of the lung. It almost always occurs in smokers between the ages of 20 and 40. Bronchoscopic interventions, such as transbronchial biopsy (TBB) and bronchoalveolar lavage (BAL), should be performed before other more invasive proce...

متن کامل

Langerhans Cell Histiocytosis Followed by Hodgkin Lymphoma: A Case Report

Langerhans cell histiocytosis (LCH) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. The major pathological features of LCH are expression of CD1a and S100 as well as Birbeck granules. Its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...

متن کامل

Langerhans Cell Histiocytosis in an Infant Mimicking a Lymphoma at Presentation

Langerhans cell histiocytosis (LCH) is a rare disorder characterized by proliferation and accumulation of clonal dendritic cells with varied clinical presentation and an unpredictable course. We report a 5-month-old infant with LCH who presented with severe respiratory distress, a large mediastinal mass, significant generalized lymphadenopathy, and hepatosplenomegaly. Lymphoma, especially T cel...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: The Egyptian Journal of Otolaryngology

سال: 2022

ISSN: ['2090-8539', '1012-5574']

DOI: https://doi.org/10.1186/s43163-022-00303-0