肺部炎性肌纤维母细胞瘤创伤性肿瘤出血

IF 0.8 Q4 RESPIRATORY SYSTEM
Takashi Yamashita, Yuta Matsubayashi, Takahiro Mochizuki
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引用次数: 0

摘要

一名有特发性癫痫病史的 23 岁女性在 5 年前的一次学校体检中发现右胸腔阴影。CT 显示右侧中叶有一薄壁空腔病变,内有一球状肿块,呈气月牙征。因癫痫发作摔倒后,她被救护车送往医院,并被收治入院。CT 显示整个右肺野弥漫性磨玻璃不透光。支气管镜检查显示支气管肺泡灌洗液带血。由于肿瘤出血,患者接受了择期单纯右肺中叶切除术,未出现并发症。最初使用ALK1克隆对ALK进行的免疫组化染色呈阴性,但随后使用D5F3和5A4克隆对ALK进行的染色呈阳性。免疫染色结果导致了炎性肌纤维母细胞瘤的诊断。患者仍在接受定期观察,术后 6 年未再复发。本病例包含两个不同的观点:一是炎性肌纤维母细胞瘤的腔隙病变可能会引起创伤性出血,应谨慎处理;二是诊断炎性肌纤维母细胞瘤时应注意克隆间染色性的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Traumatic tumor hemorrhage of inflammatory myofibroblastic tumor of the lung

A 23-year-old female with a history of idiopathic epilepsy was found to have a right chest cavity shadow in a school health checkup 5 years before. CT revealed a thin-walled cavity lesion in the right middle lobe containing a ball-like mass, showing air crescent sign. After falling due to a seizure, she was transported by ambulance and admitted. CT revealed diffuse ground-glass opacities throughout the right lung field. Bronchoscopy revealed bloody bronchial alveolar lavage fluid. Due to the tumor hemorrhage, an elective simple right middle lobe resection was performed without complications. The initial immunohistochemical staining was negative for ALK using ALK1 clone; however, subsequent staining of ALK by D5F3 and 5A4 clone was positive. Immunostaining findings led to a diagnosis of inflammatory myofibroblastic tumor. The patient remains under regular observation and has experienced no recurrence over the 6-year postoperative period. This case contains two different points: the first is that a cavity lesion of inflammatory myofibroblastic tumor may cause traumatic bleeding and should be treated with caution; the second is that attention should be paid to differences in stainability among clones when diagnosing inflammatory myofibroblastic tumor.

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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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