Blenc A M, Gómez J A, Lee M W, Torres F X, Linder J S
Department of Pathology, Henry Ford Hospital, Detroit, Michigan 48202, USA.
Am J Dermatopathol. 2000 Feb;22(1):55-9. doi: 10.1097/00000372-200002000-00011.
Phakomatous choristoma is a rare congenital lesion of the eyelid that can be clinically and/or histologically mistaken for a cyst, cutaneous adnexal neoplasm, or an ocular adnexal oncocytoma. Only 13 such cases have been previously described, mostly in the English language ophthalmic literature. Zimmerman reported the first case in 1971 and proposed the lesion to be of lenticular anlage origin, a theory that has been widely accepted. We report an additional case occurring in an 8-week-old male infant with a firm nodule of the right lower eyelid that was present since birth. A 15 x 12 x 2 mm circumscribed solid nodule with a homogenously white cut surface was surgically excised. Histologically, this lesion was comprised of cuboidal cells forming cystically dilated and irregularly branched ducts and cords within a densely fibrotic stroma. Also present were eosinophilic basement membranelike material, psammoma body-like calcifications and intraluminal degenerated ghost cells. The immunohistochemical profile of the epithelial cells included strong immunoreactivity for vimentin, focal weak staining for S-100, and negative staining for cytokeratin, epithelial membrane antigen, synaptophysin, and chromogranin. The irregularity of the ducts and cords of epithelial cells within the densely fibrotic stroma resembled an infiltrative neoplasm of cutaneous adnexal or lacrimal duct origin. However, the site of involvement, the peculiar basement membrane material, ghost cells, and immunohistochemical profile were features that helped to distinguish phakomatous choristoma from an infiltrative carcinoma. The correct identification of this lesion is essential to avoid an aggressive surgical excision, thus sparing the eyelid and lacrimal system. The purpose of this article is to bring attention to this rare entity, because it has not been described in either the dermatology or dermatopathology literature and furthermore, is not mentioned in any of the major dermatopathology texts.
晶状体异位性错构瘤是一种罕见的眼睑先天性病变,在临床和/或组织学上可能被误诊为囊肿、皮肤附属器肿瘤或眼附属器嗜酸性细胞瘤。此前仅有13例此类病例被报道,大多发表于英文眼科文献中。齐默尔曼于1971年报道了首例病例,并提出该病变起源于晶状体原基,这一理论已被广泛接受。我们报告了另外一例发生在一名8周大男婴身上的病例,其右下眼睑自出生以来就有一个坚实的结节。手术切除了一个15×12×2mm边界清晰的实性结节,其切面均匀呈白色。组织学上,该病变由立方体细胞组成,这些细胞在致密的纤维基质内形成囊状扩张且不规则分支的导管和索条。此外,还存在嗜酸性基底膜样物质、砂粒体样钙化和管腔内退变的鬼影细胞。上皮细胞的免疫组化特征包括波形蛋白强阳性、S-100局灶弱阳性,细胞角蛋白、上皮膜抗原、突触素和嗜铬粒蛋白均为阴性。致密纤维基质内上皮细胞导管和索条的不规则形态类似于皮肤附属器或泪腺导管起源的浸润性肿瘤。然而,病变部位、特殊的基底膜物质、鬼影细胞和免疫组化特征有助于将晶状体异位性错构瘤与浸润性癌区分开来。正确识别该病变对于避免激进的手术切除至关重要,从而保护眼睑和泪腺系统。本文的目的是引起对这种罕见疾病的关注,因为它在皮肤病学或皮肤病理学文献中均未被描述,而且在任何主要的皮肤病理学教科书中也未提及。