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伴有假性齐-希二氏样颗粒的先天性急性髓系白血病:一例报告

Congenital Acute Myeloid Leukaemia with Pseudo-Chediak-Higashi Like Granules: A Case Report.

作者信息

Puri Vandana, Barman Sandip, Sharma Pooja, Sikka Meera

机构信息

Assistant Professor, Department of Pathology, University College of Medical Sciences , Delhi, India .

Postgraduate, Department of Pathology, University College of Medical Sciences , Delhi, India .

出版信息

J Clin Diagn Res. 2016 Nov;10(11):ED19-ED20. doi: 10.7860/JCDR/2016/20740.8926. Epub 2016 Nov 1.

Abstract

Congenital leukaemia is a very rare entity comprising 0.8% of all childhood leukaemias. Pseudo-Chediak-Higashi Anomaly (PCHA) in acute leukaemia is a rarely described entity. However, co-existence of congenital myeloid leukaemia with PCHA is a very rare entity and to the best of our knowledge has not been described in literature till date. A full term new-born presented on the 27 day of life with severe gastroenteritis. Complete blood counts and peripheral smear examination revealed leucocytosis with presence of 76% blast cells. Approximately 15% of these blast cells showed presence of pseudo-Chediak-Higashi like granules. The diagnosis of acute myeloid leukaemia was confirmed by flow cytometry. The case report is presented due to its rarity and to highlight the differential diagnosis and clinical implications of this entity.

摘要

先天性白血病是一种非常罕见的疾病,占所有儿童白血病的0.8%。急性白血病中的假性齐-希畸形(PCHA)是一种很少被描述的疾病。然而,先天性髓系白血病与PCHA并存是一种非常罕见的情况,据我们所知,迄今为止文献中尚未有相关描述。一名足月儿在出生后第27天因严重胃肠炎就诊。全血细胞计数和外周血涂片检查显示白细胞增多,有76%的原始细胞。这些原始细胞中约15%显示存在假性齐-希畸形样颗粒。通过流式细胞术确诊为急性髓系白血病。由于该病例罕见,现予以报道,以突出该疾病的鉴别诊断及临床意义。

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本文引用的文献

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Pseudo Chediak-Higashi anomaly in acute myelomonocytic leukemia.急性粒单核细胞白血病中的假性齐-希畸形
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Pseudo-Chediak-Higashi anomaly in acute leukemia. A significant morphologic corollary?
Am J Clin Pathol. 1974 Nov;62(5):673-8. doi: 10.1093/ajcp/62.5.673.

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