Spiradenocylindromas of the skin: Tumors with morphological features of spiradenoma and cylindroma in the same lesion: Report of 12 cases

Citation
M. Michal et al., Spiradenocylindromas of the skin: Tumors with morphological features of spiradenoma and cylindroma in the same lesion: Report of 12 cases, PATHOL INT, 49(5), 1999, pp. 419-425
Citations number
33
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
PATHOLOGY INTERNATIONAL
ISSN journal
13205463 → ACNP
Volume
49
Issue
5
Year of publication
1999
Pages
419 - 425
Database
ISI
SICI code
1320-5463(199905)49:5<419:SOTSTW>2.0.ZU;2-Z
Abstract
Twelve cases of spiradenocylindromas, which revealed features of both spira denoma and cylindroma in the same tumor mass, are presented. Nine female pa tients had multiple neoplasms occurring mostly on the scalp, and two female and one male patient had a solitary cutaneous lesion. Three of the female patients with multiple cutaneous tumors had a familial history of similar c utaneous neoplasms. In one of the patient's family, the multiple cutaneous tumors were known to occur in multiple family members in four consecutive g enerations. One patient with multiple cutaneous lesions was known to have a ssociated multiple kidney cysts as confirmed by computed tomography. Histol ogically, spiradenocylindromas are composed of intermixed areas that are ei ther of typical spiradenoma in appearance or of typical cylindroma appearan ce. Apocrine and trichoepitheliomatous differentiation seen in two cases in the present series points to spiradenomas, as well as cylindromas, having complex hair follicle (folliculosebaceous apocrine) rather than eccrine dif ferentiation. The presence of lymphoid tissue was a histological feature in the present series, which was prominent in all the spiradenomatous parts o f the tumors and which was scanty or practically absent in all the cylindro matous parts. The selective presence of lymphocytes in spiradenoma and an a bsence in cylindroma suggest that spiradenomas have the unique property of attracting lymphocytes. The malignant tumors arising in three patients in t he present series had the morphology of a poorly differentiated epithelioid neoplasm. Three patients died of the disease and the other patients were e ither free of disease or alive with disease 1-30 years on follow up.