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一种进行性神经疾病,伴有获得性海蓝色组织细胞增多症,进一步支持 10 岁男孩患尼曼-皮克 C1 型的诊断。

A progressive neurological condition with acquired sea-blue histiocytosis further the diagnosis of Niemann-Pick type C1 in a 10-year-old boy.

机构信息

Department of Pediatrics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

Department of Radiology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

出版信息

Indian J Pathol Microbiol. 2020 Apr-Jun;63(2):312-314. doi: 10.4103/IJPM.IJPM_728_19.

Abstract

Sea-blue histiocytes in bone marrow can be associated with a number of conditions and have indeed often been reported in Niemann-Pick diseases, mostly in Niemann-Pick type B, but also Niemann-Pick type C. Rarely, it was reported to be related to a progressive neurological condition. In this work, early bone marrow aspirations in a boy following the discovery of hepatosplenomegaly at 1 month of age and later isolated splenomegaly did not reveal abnormal cells (which is not uncommon). Numerous sea-blue histiocytes were found in a repeated exam when the child was 10-year old, at a time he had developed a progressive neurological condition with frequent falls, clumsiness, slow and slurred speech, intellectual disability, dystonic movements, and dysphagia. Acquired sea-blue histiocytes should be considered initially on the basis of clinical symptoms. Whole-exome sequencing identified two variants in the NPC1 gene, leading to the diagnosis of Niemann-Pick type C1. This case points out the presence of sea-blue histiocytes in the bone marrow and has helped to reach a diagnosis of NPC1 which was very difficult to establish even after years of study. Given the rarity of this pathology and the variety of clinical presentations, it is important to communicate the possible forms of presentation of this syndrome.

摘要

骨髓中海蓝色组织细胞可与多种疾病相关,实际上已在尼曼-皮克病中经常报道,主要见于尼曼-皮克病 B 型,但也见于尼曼-皮克病 C 型。罕见情况下,其与进行性神经疾病相关。在这项工作中,1 个月龄时发现肝脾肿大的男孩在早期骨髓抽吸后,且之后仅表现为孤立性脾肿大,并未发现异常细胞(这并不罕见)。当患儿 10 岁时,在他出现进行性神经疾病,频繁跌倒、笨拙、言语缓慢且含糊、智力障碍、张力障碍和吞咽困难时,重复检查时发现了大量海蓝色组织细胞。根据临床症状,应首先考虑获得性海蓝色组织细胞。全外显子组测序发现 NPC1 基因中的两个变异,导致尼曼-皮克病 C1 型的诊断。该病例指出了骨髓中海蓝色组织细胞的存在,并有助于诊断 NPC1,即使经过多年研究,该诊断也非常困难。鉴于该病理学的罕见性和多种临床表现,重要的是要交流该综合征的可能表现形式。

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