Kay J M, Kahana L M, Rihal C
Department of Pathology, St. Joseph's Hospital, Hamilton Civic Hospitals, Ontario, Canada.
Hum Pathol. 1996 Sep;27(9):969-74. doi: 10.1016/s0046-8177(96)90226-9.
We describe the second example of a distinctive clinicopathologic syndrome of severe pulmonary hypertension and interstitial lung disease caused by diffuse smooth muscle proliferation of the lungs (DSMPL) occurring in a 44-year-old man of normal intelligence with no cutaneous or neurological lesions. The smooth muscle proliferation involved the walls of bronchioles, alveoli, small pulmonary arteries, and pulmonary veins. DSMPL is distinct from pulmonary lymphangioleiomyomatosis and tuberous sclerosis, and does not appear to be neoplastic or reactive. The lesions are probably best regarded as multiple hamartomas or "native benign nodular smooth muscle proliferations."
我们描述了第二例由肺部弥漫性平滑肌增生(DSMPL)引起的严重肺动脉高压和间质性肺疾病的独特临床病理综合征,该病例发生在一名44岁智力正常、无皮肤或神经病变的男性身上。平滑肌增生累及细支气管壁、肺泡、小肺动脉和肺静脉。DSMPL与肺淋巴管平滑肌瘤病和结节性硬化症不同,似乎不是肿瘤性或反应性的。这些病变可能最好被视为多发性错构瘤或“先天性良性结节性平滑肌增生”。