Wong T Y, Suster S, Nogita T, Duncan L M, Dickersin R G, Mihm M C
Dermatopathology Division, Massachusetts General Hospital, Boston.
Cancer. 1994 Mar 15;73(6):1631-43. doi: 10.1002/1097-0142(19940315)73:6<1631::aid-cncr2820730615>3.0.co;2-7.
Sweat gland carcinomas with clear cell features are extremely rare neoplasms, with few well documented cases reported in the literature.
Data on nine patients with malignant eccrine adnexal neoplasms characterized by a prominent clear cell neoplastic component were studied. Immunohistochemical stains with a panel of antibodies against epithelial, stromal, and neural antigens were performed on five tumors and electron microscopic examination of one.
The tumors showed a spectrum of histologic features and growth patterns that ranged from well differentiated, low grade malignant neoplasms to poorly differentiated, highly aggressive, recurrent, and metastasizing tumors. All tumors contained a varied proportion of cells with abundant clear cytoplasm, similar to those seen in a group of benign eccrine adnexal neoplasms that have been variously designated as clear cell hidradenoma, nodular hidradenoma, clear cell myoepithelioma, and eccrine acrospiroma. Immunohistochemical stains on five tumors and ultrastructural examination in one were consistent with eccrine differentiation. Clinical follow-up of eight patients showed local recurrence in six, followed by metastases in three, despite local excision, radiation, and chemotherapy. Criteria for differentiating these tumors from their benign counterparts and from other types of malignant adnexal neoplasms and metastatic lesions are presented.
The findings indicate that clear cell eccrine carcinomas comprise a heterogeneous group of lesions that may range from locally recurring, low grade well differentiated tumors to highly aggressive, high grade tumors with a definite potential for uncontrollable local recurrence and metastasis. Wide surgical excision is recommended as the primary treatment for such neoplasms.
具有透明细胞特征的汗腺癌是极其罕见的肿瘤,文献中报道的病例很少且记录详实。
研究了9例以显著透明细胞肿瘤成分为特征的恶性小汗腺附属器肿瘤患者的数据。对5例肿瘤进行了针对上皮、间质和神经抗原的一组抗体的免疫组织化学染色,并对其中1例进行了电子显微镜检查。
这些肿瘤表现出一系列组织学特征和生长模式,从高分化、低级别恶性肿瘤到低分化、高侵袭性、复发性和转移性肿瘤。所有肿瘤都含有不同比例的细胞质丰富的透明细胞,类似于一组被不同命名为透明细胞汗腺瘤、结节状汗腺瘤、透明细胞肌上皮瘤和小汗腺末端汗管瘤的良性小汗腺附属器肿瘤中所见的细胞。5例肿瘤的免疫组织化学染色和1例的超微结构检查均符合小汗腺分化。8例患者的临床随访显示,尽管进行了局部切除、放疗和化疗,但6例出现局部复发,其中3例发生转移。本文提出了将这些肿瘤与良性对应物、其他类型的恶性附属器肿瘤和转移性病变相鉴别的标准。
研究结果表明,透明细胞汗腺癌包括一组异质性病变,范围从局部复发的、低级别高分化肿瘤到具有明确的不可控局部复发和转移潜能的高侵袭性、高级别肿瘤。建议广泛手术切除作为此类肿瘤的主要治疗方法。