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偶然胸腺切除术中发现的多个朗格汉斯细胞结节。

Multiple Langerhans cell nodules in an incidental thymectomy.

作者信息

Novak Lea, Castro Claudia Y, Listinsky Catherine M

机构信息

Department of Surgery, University of Alabama at Birmingham, 35233, USA.

出版信息

Arch Pathol Lab Med. 2003 Feb;127(2):218-20. doi: 10.5858/2003-127-218-MLCNIA.

Abstract

The isolated appearance of Langerhans cell histiocytosis in the thymus is quite rare. We report the finding of multiple small Langerhans cell nodules in the thymus of an 11-month-old infant who had undergone thymectomy in the course of surgical correction of tetralogy of Fallot. The subtle appearance of some of these nodules and aggregates was unlike the pattern of massive thymic infiltration seen in 7 previously reported cases of thymic Langerhans cell histiocytosis in childhood. This difference led us to consider whether these aggregates might be common in the thymus but overlooked in thymus glands removed incidental to cardiac surgery. We examined histologic material from 22 sequential thymectomy specimens removed during cardiac surgery from infants and children. None (0/22) had cohesive aggregates of Langerhans cells, as were seen in the index patient's thymus. Our patient's small thymic nodules resemble more closely a pattern found in adult patients with myasthenia gravis who have been incidentally shown to have Langerhans cell histiocytosis.

摘要

朗格汉斯细胞组织细胞增多症单独出现在胸腺的情况相当罕见。我们报告了一名11个月大婴儿胸腺中多个小朗格汉斯细胞结节的发现,该婴儿在法洛四联症手术矫正过程中接受了胸腺切除术。这些结节和聚集物中一些的细微表现与之前报道的7例儿童胸腺朗格汉斯细胞组织细胞增多症中所见的大量胸腺浸润模式不同。这种差异使我们思考这些聚集物在胸腺中是否可能很常见,但在心脏手术中 incidental 切除的胸腺中被忽视了。我们检查了22例在心脏手术中从婴幼儿和儿童身上连续切除的胸腺标本的组织学材料。没有一个(0/22)有朗格汉斯细胞的凝聚性聚集物,就像在索引患者的胸腺中看到的那样。我们患者的小胸腺结节更类似于在偶然发现患有朗格汉斯细胞组织细胞增多症的成年重症肌无力患者中发现的一种模式。 (注:原文中“incidental”有误,推测可能是“incidentally”,翻译时按推测修正了。)

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