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全身性播散性朗格汉斯细胞组织细胞增生症伴间变性大细胞淋巴瘤激酶阳性:病例报告。

Anaplastic lymphoma kinase-positive histiocytosis with multisystem involvement: A case report.

机构信息

Department of Dermatology, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

Pediatr Dermatol. 2024 May-Jun;41(3):551-553. doi: 10.1111/pde.15546. Epub 2024 Feb 12.

DOI:10.1111/pde.15546
PMID:38346136
Abstract

Anaplastic lymphoma kinase (ALK)-positive histiocytosis is a rare disease that usually occurs in infants and young children and is characterized by ALK-positive histiocytes infiltrating organs. We present a case of multisystem involvement of ALK-positive histiocytosis in a female infant with skin nodules as the initial presentation. Despite multiorgan involvement, most tumors had spontaneously regressed, and all bones were partially healed after 40 months of regular follow-up without treatment. However, gait abnormalities persisted, indicating that early treatment may have greater impact in maintaining a child's quality of life when the disease involves the brain or the critical period of bone development.

摘要

间变性淋巴瘤激酶(ALK)阳性组织细胞增生症是一种罕见疾病,通常发生于婴儿和幼儿,其特征是 ALK 阳性组织细胞浸润各器官。我们报告了一例女性婴儿以皮肤结节为首发表现的 ALK 阳性组织细胞增生症多系统受累病例。尽管存在多器官受累,但大多数肿瘤自发消退,所有骨骼在未经治疗的情况下经过 40 个月的定期随访后部分愈合。然而,步态异常仍存在,这表明当疾病累及大脑或骨骼发育关键期时,早期治疗可能对维持儿童的生活质量有更大影响。

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Anaplastic lymphoma kinase-positive histiocytosis with multisystem involvement: A case report.全身性播散性朗格汉斯细胞组织细胞增生症伴间变性大细胞淋巴瘤激酶阳性:病例报告。
Pediatr Dermatol. 2024 May-Jun;41(3):551-553. doi: 10.1111/pde.15546. Epub 2024 Feb 12.
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