[A case of primary endobronchial mucosa-associated lymphoid tissue lymphoma with middle lobe atelectasis].

Nihon Kyobu Shikkan Gakkai zasshi Pub Date : 1997-11-01
Y Naya, M Ohe, M Fujino, Y Akiyama, T Kirisawa, Y Kawakami
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引用次数: 0

Abstract

A 60-year-old woman was admitted for evaluation of an abnormal shadow in her chest X-ray. A chest roentgenogram revealed middle lobe atelectasis and a tomogram showed masses mainly in the right intermediate bronchus. In bronchoscopy, the bronchus was severely narrowed by irregularly surfaced masses. Microscopic examinations of transbronchial biopsy specimen showed the mucosal and submucosal tissue diffusedly infiltrated mainly by lymphocytes composed of small lymphocytes, centrocyte-like cells and monocytoid cells. The B-cell origin was suggested by a positive L-26 stain. Monoclonality of lymphocytes was proven by Southern blot analysis and in situ hybridization. The diagnosis was primary endobronchial lymphoma of mucosa-associated lymphoid tissue. The case was treated with chemotherapy protocol (CAMBO-VIP) and has been in complete remission for 20 months.

[原发性支气管黏膜相关淋巴组织淋巴瘤合并中肺不张1例]。
一名60岁妇女因胸部x光检查异常阴影而入院。胸部x线摄影显示中肺不张,断层摄影显示肿块主要位于右中间支气管。在支气管镜检查中,支气管被不规则表面的肿块严重变窄。经支气管活检标本镜检显示粘膜及粘膜下组织弥漫性浸润主要为淋巴细胞,由小淋巴细胞、中心细胞样细胞和单核细胞组成。L-26染色阳性提示b细胞来源。经Southern blot和原位杂交证实淋巴细胞单克隆性。诊断为黏膜相关淋巴组织的原发性支气管内淋巴瘤。该病例接受化疗方案(柬埔寨- vip)治疗,已完全缓解20个月。
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