Pulmonary Blastoma in an adult male

M. Alim, Dina Abo Alam, Y. Sayed, Amr Abdellateef, El Sayed Al Ghareeb, Mohammad Nafee, M. Sayed, Sami Ba Baker, Mohammad Badry Eid, Suzan A. Mageed, S. E. Sayed
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Abstract

Pulmonary blastoma is one of the rare lung tumors and is considered to be distinct from other lung tumors by its pathological features, clinical course and prognosis [1]. Classic pulmonary blastoma is composed of both malignant mesenchymal stroma and epithelial components resembling embryonic lung tissue. Surgery is the standard treatment and the efficacy of adjuvant chemotherapy and radiotherapy has not yet been established [2]. Case Report Our patient was admitted and managed at Abassia Pulmonary Hospital, Ministry of Health, Cairo Governorate, Egypt. A 37-year-old Egyptian male presented to our hospital after repeated attacks of blood tinged sputum. The first attack dated about 6 months before admission. The patient had progressive shortness of breath over a period of two years. The patient was a smoker of one pack of cigarettes per day for more than 15 years. There was no significant past history nor family history. After admission to the Chest Medicine Department at Abbasia Pulmonary Hospital, routine basic investigations were done including complete blood picture with differential count, fasting blood sugar and 2 hours after meal, liver function tests, renal function tests, and coagulation profile. All investigations were within normal.
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成年男性肺母细胞瘤
肺母细胞瘤是一种罕见的肺部肿瘤,其病理特征、临床病程和预后被认为是区别于其他肺部肿瘤的[1]。典型的肺母细胞瘤由恶性间充质间质和类似胚胎肺组织的上皮成分组成。手术是标准治疗方法,辅助化疗和放疗的疗效尚未确定[2]。病例报告:本例患者在埃及开罗省卫生部Abassia肺病医院接受治疗。一名37岁埃及男性因痰中带血反复发作而来我院就诊。第一次发作发生在入院前六个月。患者在两年的时间里出现进行性呼吸短促。患者是一个吸烟者,每天一包烟超过15年。没有明显的既往病史和家族史。入院后进行常规基础检查,包括全血计数、空腹血糖及餐后2小时血糖、肝功能检查、肾功能检查、凝血检查。所有调查均在正常范围内。
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