Singer G, Haag E, Anabitarte M
Institute of Pathology, Cantonal Hospital, Baden, Switzerland.
Histopathology. 1998 Jan;32(1):60-2. doi: 10.1046/j.1365-2559.1998.00337.x.
We describe the clinical and pathological findings of a previously unreported cutaneous lung tissue heterotopia in a child.
The 3-year-old female patient developed a 8-mm secreting papule over her left scapula. Pathological examination revealed a lesion composed of bronchioles and alveoli within the subcutis and the dermis, with bronchiolar connection to the epidermis. Alveolar type II cells indicating full pulmonary differentiation were detected with a monoclonal antibody (AMH 152).
The described features suggest that this lesion is a unique variant of rarely observed bronchus-like entities of the skin, designated as cutaneous bronchogenic cysts or cutaneous branchial cleft cysts.
我们描述了一名儿童中一种此前未报告的皮肤肺组织异位的临床和病理表现。
一名3岁女性患者在左肩胛骨处出现一个8毫米的分泌性丘疹。病理检查显示，皮下组织和真皮内有由细支气管和肺泡组成的病变，细支气管与表皮相连。用单克隆抗体（AMH 152）检测到了表明完全肺分化的II型肺泡细胞。
所描述的特征表明，该病变是皮肤中罕见的支气管样实体的一种独特变体，称为皮肤支气管源性囊肿或皮肤鳃裂囊肿。
