Scheman A J, Ray D J, Witkop C J, Dahl M V
Department of Dermatology, University of Minnesota Medical Center, Minneapolis.
J Am Acad Dermatol. 1989 Aug;21(2 Pt 2):351-7.
Hereditary mucoepithelial dysplasia, a dyshesive, dyskeratotic epithelial syndrome caused by an abnormality in desmosomes and gap junctions, involves the mucosae, skin, hair, eyes, and lungs. A 16-year-old patient had nontender, fire-red mucosae; keratosis pilaris; diffuse, nonscarring alopecia; cataracts; photophobia; corneal vascularization; and decreased visual acuity. Histologic examination of gingival sections showed a dyshesive epithelium with atrophy, dyskeratosis, lack of keratinization, and unusual cytoplasmic inclusions. Results of electron microscopic studies showed a reduced number of desmosomes, amorphous intercellular material, and cytoplasmic inclusions resembling tonofilaments and gap junction material. The patient described in this report represents an apparently sporadic case of hereditary mucoepithelial dysplasia. Other cases described previously in the literature are reviewed. We believe this disorder should be brought to the attention of dermatologists because patients with hereditary mucoepithelial dysplasia have numerous skin problems and are susceptible to recurrent infection and potentially fatal bullous lung disease. Also, misinterpreted abnormal results from cervical Pap smears could lead to hysterectomy being performed unnecessarily on these patients.
遗传性黏液上皮发育异常是一种由桥粒和缝隙连接异常引起的上皮黏附不良、角化异常综合征,累及黏膜、皮肤、毛发、眼睛和肺部。一名16岁患者有不痛的火红色黏膜;毛发角化病;弥漫性非瘢痕性脱发;白内障;畏光;角膜血管化;以及视力下降。牙龈切片的组织学检查显示上皮黏附不良,伴有萎缩、角化异常、无角化现象以及异常的细胞质内含物。电子显微镜研究结果显示桥粒数量减少、无定形细胞间物质以及类似张力丝和缝隙连接物质的细胞质内含物。本报告中描述的患者代表了一例明显散发的遗传性黏液上皮发育异常病例。对文献中先前描述的其他病例进行了综述。我们认为这种疾病应引起皮肤科医生的注意,因为遗传性黏液上皮发育异常患者有许多皮肤问题,易发生反复感染和潜在致命的大疱性肺病。此外,宫颈巴氏涂片检查结果异常被误判可能导致对这些患者不必要地进行子宫切除术。