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新生儿先天性自愈性网状组织细胞增生症(桥本-普利茨克病)

Congenital self healing reticulohistiocytosis in a newborn (Hashimoto Pritzker).

作者信息

Orle Joana, Mósca Ana Maria, Sousa Maria Auxiliadora Jeunon, Lima Cíntia Maria Oliveira, Adriano André Ricardo, Rezende Patrícia Makino

机构信息

Policlínica Geral do Rio de Janeiro, Instituto de Pós-Graduação Médica Carlos Chagas, Rio de Janeiro, Brasil.

出版信息

An Bras Dermatol. 2011 Jul-Aug;86(4):785-8. doi: 10.1590/s0365-05962011000400026.

DOI:10.1590/s0365-05962011000400026
PMID:21987150
Abstract

Congenital self-healing reticulohistiocytosis is the benign spectrum of Langerhans Cell Histiocytosis, characterized by cutaneous lesions at birth or in the neonatal period, absence of systemic manifestations and spontaneous resolution of clinical status. Despite the benign and often self-resolving course in most patients, studies show that in some cases there may be metastasis or recurrence of the disease, emphasizing that the clinical course is variable, requiring long-term follow-up. The monitoring of the patient for a long period is important to detect possible systemic involvement, as there is a report of recurrence involving the skin, mucosa, bone and pituitary gland.

摘要

先天性自愈性网状组织细胞增生症是朗格汉斯细胞组织细胞增生症的良性类型,其特征为出生时或新生儿期出现皮肤病变,无全身表现且临床状况可自发缓解。尽管大多数患者病程呈良性且常可自愈,但研究表明,在某些情况下该病可能会转移或复发,这强调了临床病程具有变异性,需要长期随访。对患者进行长期监测对于发现可能的全身受累情况很重要,因为有报告称复发累及皮肤、黏膜、骨骼和垂体。

相似文献

1
Congenital self healing reticulohistiocytosis in a newborn (Hashimoto Pritzker).新生儿先天性自愈性网状组织细胞增生症(桥本-普利茨克病)
An Bras Dermatol. 2011 Jul-Aug;86(4):785-8. doi: 10.1590/s0365-05962011000400026.
2
[Solitary congenital self-healing histiocytosis (Hashimoto-Pritzker disease)].[孤立性先天性自愈性组织细胞增多症(桥本-普利茨克病)]
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[Blueberry Muffin Baby and Langerhans' congenital cell histiocytosis].[蓝莓松饼宝宝与朗格汉斯先天性细胞组织细胞增多症]
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Congenital self-healing reticulohistiocytosis in a newborn: unusual oral and cutaneous manifestations.新生儿先天性自限性网状组织细胞增生症:不常见的口腔和皮肤表现。
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Congenital "self-healing" Langerhans cell histiocytosis (Hashimoto-Pritzker disease): a report of two cases with the same cutaneous manifestations but different clinical course.先天性“自愈性”朗格汉斯细胞组织细胞增多症(桥本-普里茨克病):两例皮肤表现相同但临床病程不同的病例报告。
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Congenital self-healing histiocytosis (Hashimoto-Pritzker).先天性自愈性组织细胞增生症(桥本-普利茨克病)
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Congenital self-healing reticulohistiocytosis with spontaneous regression.先天性自愈性网状组织细胞增生症伴自发消退。
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引用本文的文献

1
Congenital self-healing reticulohistiocytosis in a newborn: unusual oral and cutaneous manifestations.新生儿先天性自限性网状组织细胞增生症:不常见的口腔和皮肤表现。
Ital J Pediatr. 2021 Jun 10;47(1):135. doi: 10.1186/s13052-021-01082-9.
2
Congenital self-healing langerhans cell histiocytosis: clinical and pathological characteristics.先天性自愈性朗格汉斯细胞组织细胞增多症:临床与病理特征
Int J Clin Exp Pathol. 2019 Jun 1;12(6):2275-2278. eCollection 2019.
3
LATE-ONSET SELF-HEALING LANGERHANS CELL HISTIOCYTOSIS: REPORT OF A VERY RARE ENTITY.
迟发性自愈性朗格汉斯细胞组织细胞增多症:一种极其罕见病例的报告
Rev Paul Pediatr. 2017 Jan-Mar;35(1):115-119. doi: 10.1590/1984-0462/;2017;35;1;00015.
4
Case for diagnosis. Hashimoto-Pritzker disease.诊断病例。桥本-普里茨克病。
An Bras Dermatol. 2013 Nov-Dec;88(6):1001-3. doi: 10.1590/abd1806-4841.20132451.