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深部幼年性黄色肉芽肿的细胞学特征。

Cytologic features of deep juvenile xanthogranuloma.

作者信息

Grenko R T, Sickel J Z, Abendroth C S, Cilley R E

机构信息

Department of Pathology, Hershey Medical Center, PA 17033, USA.

出版信息

Diagn Cytopathol. 1996 Nov;15(4):329-33. doi: 10.1002/(SICI)1097-0339(199611)15:4<329::AID-DC15>3.0.CO;2-Q.

Abstract

Juvenile xanthogranuloma (JXG) is a rare lesion of the skin and deep tissues whose cytologic features have not previously been published. We report on 2 cases of JXG in patients aged 5 days and 5 yr who presented with an axillary mass and enlarged supraclavicular lymph node, respectively. Fine-needle aspiration and touch imprints made from the surgical biopsies yielded cellular specimens composed of histiocytes, multinucleated Touton-type giant cells, and variable admixtures of lymphocytes and eosinophils. One lesion was composed primarily of benign-appearing histiocytes with admixed multinucleated giant cells and a few lymphocytes. The second lesion consisted of a few histiocytes, occasional Touton giant cells, many lymphocytes, and scattered fibroblasts. The histiocytes were CD68-positive and S100-negative. Histologic follow-up confirmed the diagnosis of juvenile xanthogranuloma. One patient was lost to follow-up; the other is alive without evidence of recurrence 1 yr after surgery. We conclude that deep JXG has characteristic and diagnostic cytologic features.

摘要

幼年性黄色肉芽肿(JXG)是一种罕见的皮肤和深部组织病变,其细胞学特征此前尚未见报道。我们报告了2例JXG患者,分别为5天和5岁,前者表现为腋窝肿块,后者表现为锁骨上淋巴结肿大。手术活检的细针穿刺和触摸印片得到了由组织细胞、多核Touton型巨细胞以及淋巴细胞和嗜酸性粒细胞不同比例混合组成的细胞标本。一个病变主要由外观良性的组织细胞组成,伴有多核巨细胞和少量淋巴细胞。第二个病变由少量组织细胞、偶见的Touton巨细胞、许多淋巴细胞和散在的成纤维细胞组成。组织细胞CD68阳性,S100阴性。组织学随访证实为幼年性黄色肉芽肿。1例患者失访;另1例患者术后1年存活,无复发迹象。我们得出结论,深部JXG具有特征性的诊断细胞学特征。

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