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纵隔非典型类癌与1型神经纤维瘤病

Mediastinal atypical carcinoid and neurofibromatosis type 1.

作者信息

Mathew P, Roberts J A, Zwischenberger J, Haque A K

机构信息

Division of Medical Oncology, Thoracic Surgery and Pathology, University of Texas Medical Branch, Galveston, Texas, USA.

出版信息

Arch Pathol Lab Med. 2000 Feb;124(2):319-21. doi: 10.5858/2000-124-0319-MACANT.

Abstract

We report a case of mediastinal atypical carcinoid in a 63-year-old woman with neurofibromatosis type 1 (NF-1), who presented with shortness of breath and a bulky mediastinal mass. Initial consideration was given to a neurogenic tumor. However, on thoracoscopic biopsy, the histologic appearance was consistent with an atypical carcinoid. Carcinoid tumors have been reported in association with NF-1 previously, but commonly in such unusual sites as the ampulla of Vater and duodenum and not in the thorax. The bulky, extensive, and highly vascular nature of the lesion precluded resection or debulking surgery. To our knowledge, there are no previous reports of atypical carcinoid of the lung or mediastinum in a patient with neurofibromatosis. This case report, therefore extends the spectrum of solid neoplasia in general and carcinoid tumors in specific, as they occur in association with NF-1.

摘要

我们报告一例63岁患有1型神经纤维瘤病(NF-1)的女性纵隔非典型类癌,该患者表现为呼吸急促和纵隔巨大肿块。最初考虑为神经源性肿瘤。然而,经胸腔镜活检,组织学表现符合非典型类癌。类癌肿瘤此前已有与NF-1相关的报道,但通常发生在诸如 Vater壶腹和十二指肠等不寻常部位,而非胸部。病变体积大、范围广且血管丰富,无法进行切除或减瘤手术。据我们所知,此前尚无神经纤维瘤病患者发生肺或纵隔非典型类癌的报道。因此,本病例报告扩展了一般实体瘤尤其是与NF-1相关的类癌肿瘤的范围。

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