Corsi A, Salvi P F, Diomesi Camassei F, Bosman C
Dipartimento di Medicina Sperimentale e Patologia, Università La Sapienza di Roma.
Pathologica. 1997 Oct;89(5):536-9.
Penis calcinosis is a rare pathology and only two previous cases have been reported in literature. We describe the clinicopathologic features of a case of nodular foreskin calcinosis in a 25-year-old man. The patient's history resulted negative for local trauma, inflammatory disorders or metabolic diseases. The mass measured up to 2 cm and was histologically constituted by multiple intradermic calcium deposits, whose deepest ones were surrounded by epithelioid histiocytes and multinucleated giant cells, with no evidence of any epithelial structures around none of them. These features were consistent with a non-metastatic calcinosis, likely idiopathic, even though also dystrophic calcinosis, observed at its end-stage, may show the same microscopic aspect. The exact idiopathic/dystrophic nosology is briefly discussed.
阴茎钙化是一种罕见的病理情况,文献中仅报道过两例。我们描述了一名25岁男性结节性包皮钙化病例的临床病理特征。患者既往史显示无局部创伤、炎症性疾病或代谢性疾病。肿块最大达2厘米,组织学上由多个真皮内钙沉积构成,最深层的钙沉积被上皮样组织细胞和多核巨细胞围绕,周围均未发现任何上皮结构。这些特征符合非转移性钙化,可能为特发性,尽管在终末期观察到的营养不良性钙化也可能呈现相同的微观表现。本文简要讨论了确切的特发性/营养不良性分类。