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源自尼曼-匹克病的继发性海蓝色组织细胞增生症。

Secondary sea-blue histiocytosis derived from Niemann-Pick disease.

作者信息

Suzuki Osamu, Abe Masafumi

机构信息

First Department of Pathology, School of Medicine, Fukushima Medical University, Fukushima, Japan.

出版信息

J Clin Exp Hematop. 2007 Apr;47(1):19-21. doi: 10.3960/jslrt.47.19.

DOI:10.3960/jslrt.47.19
PMID:17510534
Abstract

Sea-blue histiocytosis is a rare disorder seen in patients with lipid metabolic or ceroid storage diseases. Sea-blue histiocytes are ceroid-laden macrophages detectable by May-Giemsa staining. We report a case of a 28-year-old woman diagnosed with Niemann-Pick disease at 2 or 3 years of age. To confirm this diagnosis, we examined her bone marrow, which revealed scattered foci containing aggregates of foamy macrophages. May-Giemsa staining identified blue-staining foamy macrophages, referred to as sea-blue histiocytes. In summary, we report the detection of sea-blue histiocytosis in an adult with Niemann-Pick disease.

摘要

海蓝色组织细胞增生症是一种罕见的疾病,见于脂质代谢或类蜡质贮积病患者。海蓝色组织细胞是经美吉姆萨染色可检测到的含类蜡质的巨噬细胞。我们报告一例28岁女性病例,该患者在2或3岁时被诊断为尼曼-匹克病。为证实这一诊断,我们检查了她的骨髓,发现有散在病灶,其中含有泡沫状巨噬细胞聚集物。美吉姆萨染色鉴定出蓝色染色的泡沫状巨噬细胞,即海蓝色组织细胞。总之,我们报告了在一名成年尼曼-匹克病患者中检测到海蓝色组织细胞增生症。

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1
Secondary sea-blue histiocytosis derived from Niemann-Pick disease.源自尼曼-匹克病的继发性海蓝色组织细胞增生症。
J Clin Exp Hematop. 2007 Apr;47(1):19-21. doi: 10.3960/jslrt.47.19.
2
Sea-blue histiocytosis secondary to Niemann-Pick disease type B: a case report.B型尼曼-匹克病继发海蓝色组织细胞增多症:一例报告
Ann Hematol. 2001 Oct;80(10):620-2. doi: 10.1007/s002770100354.
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A progressive neurological condition with acquired sea-blue histiocytosis further the diagnosis of Niemann-Pick type C1 in a 10-year-old boy.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。
Indian J Pathol Microbiol. 2020 Apr-Jun;63(2):312-314. doi: 10.4103/IJPM.IJPM_728_19.
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Liver lesion on computed tomography and ultrasonography in adult Niemann Pick disease related to sea blue histiocyte syndrome--a case report.成人尼曼-匹克病合并海蓝组织细胞综合征的肝脏病变:计算机断层扫描和超声检查结果——病例报告
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Adult Niemann-Pick disease masquerading as sea blue histiocyte syndrome: report of a case confirmed by lipid analysis and enzyme assays.伪装成海蓝组织细胞综合征的成人尼曼-匹克病:一例经脂质分析和酶测定确诊的病例报告
Am J Hematol. 1985 Dec;20(4):391-400. doi: 10.1002/ajh.2830200411.
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Sea-blue histiocytosis in a family with Niemann-Pick disease. A clinical, morphological and biochemical study.患有尼曼-匹克病家族中的海蓝色组织细胞增生症。一项临床、形态学及生化研究。
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Sea-blue histiocytes in bone marrow of patient with Niemann-Pick disease type B.B型尼曼-匹克病患者骨髓中的海蓝色组织细胞。
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[Neurovisceral deposits with supranuclear ophthalmoplegia of vertical movements and presence in the bone marrow of blue histiocytes or Neville's disease. Report of two cases].[伴有垂直运动核上性眼肌麻痹及骨髓中出现蓝色组织细胞或内维尔病的神经内脏沉积。两例报告]
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Syndrome of the sea-blue histiocyte.海蓝色组织细胞综合征
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Sea-blue histiocyte syndrome in bone marrow secondary to total parenteral nutrition including fat-emulsion sources: a clinicopathologic study of seven cases.
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Secondary Sea-Blue Histiocytosis in a Patient with Transfusion Dependent HbE-Beta Thalassaemia and Osteosarcoma.一名依赖输血的血红蛋白E-β地中海贫血和骨肉瘤患者的继发性海蓝色组织细胞增多症
Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):262-6. doi: 10.1007/s12288-015-0582-6. Epub 2015 Aug 29.
2
Unusually prominent horizontal gaze palsy in a case of Niemann-Pick type C disease.1例尼曼-匹克C型病患者出现异常明显的水平凝视麻痹。
Ann Indian Acad Neurol. 2013 Apr;16(2):279-81. doi: 10.4103/0972-2327.112498.