A Case of Multifocal Lymphangioendotheliomatosis With Thrombocytopenia and Changes in Coagulopathy

Author:

Nagao Daiki1,Ozeki Michio1,Nozawa Akifumi12,Yasue Shiho1,Sasai Hideo1,Endo Saori1,Kato Takazumi3,Hori Yumiko45,Ohnishi Hidenori1

Affiliation:

1. Department of Pediatrics

2. Department of Medical Genetics, Tohoku University School of Medicine, Sendai

3. Department of Digestive Surgery and Pediatric Surgery, Gifu University Graduate School of Medicine, Gifu

4. Department of Pathology, Osaka University Graduate School of Medicine

5. Department of Central Laboratory and Surgical Pathology, National Hospital Organization, Osaka National Hospital, Osaka, Japan

Abstract

Multifocal lymphangioendotheliomatosis with thrombocytopenia is a rare disease characterized by progressive multiple vascular lesions and is accompanied by thrombocytopenia. The precise diagnosis of this disease is frequently difficult because of the heterogeneity of the clinical symptoms. We report a case of a male infant who presented with severe thrombocytopenia induced by local inflammation. In addition, enlargement of the extremities with soft tissue and bone involvement without gastrointestinal bleeding was observed. The thrombocytopenia resolved after a combination therapy of sirolimus and prednisolone. Our finding that plasma angiopoietin-2 concentrations reflected the disease status suggests its utility as a biomarker of Multifocal lymphangioendotheliomatosis with thrombocytopenia.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Immune-globulin/sirolimus;Reactions Weekly;2023-11-11

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