Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a clonal histiocytic disorder. The variable clinical manifestations from isolated bone lesion to multisystem disease can cause difficulties and delay in diagnosis. We report a 2 years and 8 months-old girl who presented with a 2 weeks history of persistent f...

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Main Authors: Omayma SEB, Fauzana K, Aisyah MR, Noraidah M, Noor Hamidah Hussin
Format: Article
Language:en
Published: Pusat Perubatan Universiti Kebangsaan Malaysia 2018
Online Access:http://journalarticle.ukm.my/20214/1/21_ms0165_pdf_62838.pdf
http://journalarticle.ukm.my/20214/
https://www.medicineandhealthukm.com/toc/13/1
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author Omayma SEB,
Fauzana K,
Aisyah MR,
Noraidah M,
Noor Hamidah Hussin,
author_facet Omayma SEB,
Fauzana K,
Aisyah MR,
Noraidah M,
Noor Hamidah Hussin,
author_sort Omayma SEB,
building Tun Sri Lanang Library
collection Institutional Repository
content_provider Universiti Kebangsaan Malaysia
content_source UKM Journal Article Repository
continent Asia
country Malaysia
description Langerhans cell histiocytosis (LCH) is a clonal histiocytic disorder. The variable clinical manifestations from isolated bone lesion to multisystem disease can cause difficulties and delay in diagnosis. We report a 2 years and 8 months-old girl who presented with a 2 weeks history of persistent fever and weight loss associated with progressive abdominal distension. Physical examination revealed pallor, bilateral proptosis, seaborrheic dermatitis over the scalp and hepatosplenomegaly. Skull X-ray demonstrated multiple lytic lesions at the base and the skull vault. Bone marrow morphology showed numerous abnormal Langerhans cells (LCs) and foamy macrophages. The trephine immunohistochemistry (IHC) stains for CD1a, S-100 and CD68 were inconclusive. The diagnosis of multisystem Langerhans cell histiocytosis (MS-LCH) in this patient was based on the clinical presentation, radiological and morphological analysis. She subsequently received chemotherapy and currently she is on maintenance therapy with a good clinical response. LCH is a rare disease and although the IHC was inconclusive, the correlation of clinical, radiological and morphological data are essential for the diagnosis.
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language en
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spelling my-ukm.journal.202142022-10-21T08:36:11Z http://journalarticle.ukm.my/20214/ Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis Omayma SEB, Fauzana K, Aisyah MR, Noraidah M, Noor Hamidah Hussin, Langerhans cell histiocytosis (LCH) is a clonal histiocytic disorder. The variable clinical manifestations from isolated bone lesion to multisystem disease can cause difficulties and delay in diagnosis. We report a 2 years and 8 months-old girl who presented with a 2 weeks history of persistent fever and weight loss associated with progressive abdominal distension. Physical examination revealed pallor, bilateral proptosis, seaborrheic dermatitis over the scalp and hepatosplenomegaly. Skull X-ray demonstrated multiple lytic lesions at the base and the skull vault. Bone marrow morphology showed numerous abnormal Langerhans cells (LCs) and foamy macrophages. The trephine immunohistochemistry (IHC) stains for CD1a, S-100 and CD68 were inconclusive. The diagnosis of multisystem Langerhans cell histiocytosis (MS-LCH) in this patient was based on the clinical presentation, radiological and morphological analysis. She subsequently received chemotherapy and currently she is on maintenance therapy with a good clinical response. LCH is a rare disease and although the IHC was inconclusive, the correlation of clinical, radiological and morphological data are essential for the diagnosis. Pusat Perubatan Universiti Kebangsaan Malaysia 2018 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/20214/1/21_ms0165_pdf_62838.pdf Omayma SEB, and Fauzana K, and Aisyah MR, and Noraidah M, and Noor Hamidah Hussin, (2018) Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis. Medicine & Health, 13 (1). pp. 220-226. ISSN 2289-5728 https://www.medicineandhealthukm.com/toc/13/1
spellingShingle Omayma SEB,
Fauzana K,
Aisyah MR,
Noraidah M,
Noor Hamidah Hussin,
Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title_full Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title_fullStr Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title_full_unstemmed Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title_short Importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
title_sort importance of clinical and morphological correlations in diagnosing langerhans cell histiocytosis
url http://journalarticle.ukm.my/20214/1/21_ms0165_pdf_62838.pdf
http://journalarticle.ukm.my/20214/
https://www.medicineandhealthukm.com/toc/13/1
url_provider http://journalarticle.ukm.my/