Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series
Langerhans cell histiocytosis (LCH) is a rare childhood hematopoietic disease, and hence, there are few reports summarizing the course leading to the diagnosis. We described the initial symptoms and the clinical course of LCH. We carried out a retrospective review of charts from a single medical cen...
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Online Access: | https://doi.org/10.1177/2333794X19857377 |
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doaj-f69a73ac2b9f4dc78c8b42f8017429402020-11-25T02:47:51ZengSAGE PublishingGlobal Pediatric Health2333-794X2019-06-01610.1177/2333794X19857377Initial Symptoms of Langerhans Cell Histiocytosis: A Case SeriesYukari Atsumi MD0Yuya Saito MD1Hiroshi Hataya MD2Yuki Yuza MD3Department of General Pediatrics, Tokyo Metropolitan Children’s Medical Center, Tokyo, JapanDepartment of Hematology and Oncology, Tokyo Metropolitan Children’s Medical Center, Tokyo, JapanDepartment of General Pediatrics, Tokyo Metropolitan Children’s Medical Center, Tokyo, JapanDepartment of Hematology and Oncology, Tokyo Metropolitan Children’s Medical Center, Tokyo, JapanLangerhans cell histiocytosis (LCH) is a rare childhood hematopoietic disease, and hence, there are few reports summarizing the course leading to the diagnosis. We described the initial symptoms and the clinical course of LCH. We carried out a retrospective review of charts from a single medical center, and 21 patients with the diagnosis of LCH were enrolled. The initial symptoms of 16 cases were caused by bone lesions; of these cases, there were 8 instances of soft tissue swelling as the initial symptom (38%) and 8 instances of bone pain without swelling (38%). Among the cases of bone lesion, 4 of 6 cases of skull lesion were painless while all vertebral body lesions and long bone lesions were accompanied by pain. LCH bone lesions caused various symptoms depending on the site of the lesion and this makes the diagnosis difficult. A detailed physical examination and imaging studies are recommended for early diagnosis.https://doi.org/10.1177/2333794X19857377 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yukari Atsumi MD Yuya Saito MD Hiroshi Hataya MD Yuki Yuza MD |
spellingShingle |
Yukari Atsumi MD Yuya Saito MD Hiroshi Hataya MD Yuki Yuza MD Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series Global Pediatric Health |
author_facet |
Yukari Atsumi MD Yuya Saito MD Hiroshi Hataya MD Yuki Yuza MD |
author_sort |
Yukari Atsumi MD |
title |
Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series |
title_short |
Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series |
title_full |
Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series |
title_fullStr |
Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series |
title_full_unstemmed |
Initial Symptoms of Langerhans Cell Histiocytosis: A Case Series |
title_sort |
initial symptoms of langerhans cell histiocytosis: a case series |
publisher |
SAGE Publishing |
series |
Global Pediatric Health |
issn |
2333-794X |
publishDate |
2019-06-01 |
description |
Langerhans cell histiocytosis (LCH) is a rare childhood hematopoietic disease, and hence, there are few reports summarizing the course leading to the diagnosis. We described the initial symptoms and the clinical course of LCH. We carried out a retrospective review of charts from a single medical center, and 21 patients with the diagnosis of LCH were enrolled. The initial symptoms of 16 cases were caused by bone lesions; of these cases, there were 8 instances of soft tissue swelling as the initial symptom (38%) and 8 instances of bone pain without swelling (38%). Among the cases of bone lesion, 4 of 6 cases of skull lesion were painless while all vertebral body lesions and long bone lesions were accompanied by pain. LCH bone lesions caused various symptoms depending on the site of the lesion and this makes the diagnosis difficult. A detailed physical examination and imaging studies are recommended for early diagnosis. |
url |
https://doi.org/10.1177/2333794X19857377 |
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