Goldblum J R, Hart W R
Department of Anatomic Pathology, The Cleveland Clinic Foundation, Ohio 44195, USA.
Am J Surg Pathol. 1998 Feb;22(2):170-9. doi: 10.1097/00000478-199802000-00004.
Perianal Paget's disease is rare, and its relationship to an associated internal regional cancer has been ill defined. We analyzed the histologic and immunohistochemical features of perianal Paget's disease in 11 patients to determine the frequency and relationship of associated regional internal carcinoma and to gain insight into its histogenesis. Of five patients with documented rectal adenocarcinoma, it was discovered synchronously with the Paget's disease in four and, subsequently, in one. Paget's cells of signet ring type predominated in four cases. Intraepithelial glands with intraluminal dirty necrosis were present in four cases. The immunophenotype in four cases studied was cytokeratin (CK)7+/CK20+/gross cystic disease fluid protein- (GCDFP) in both the intraepithelial Paget's cells and the invasive rectal adenocarcinoma. Six patients did not have documented rectal carcinoma. The Paget's cells in four were CK7+/CK20-/GCDFP15+. Three of these had purely intraepithelial Paget's disease, and invasive or metastatic disease developed in none after wide local excision. Bilateral inguinal lymph node metastases developed in the fourth patient, and the patient died 8 months after diagnosis of Paget's disease. In two patients, the Paget's cells were CK7+/CK20+/GCDFP15-. Recurrent intraepithelial perianal Paget's disease developed in one patient at 7 months; the patient was alive without disease at 24 months, and the other patient had several intraepithelial recurrences of perianal Paget's disease, and, subsequently, a large perianal tumor of uncertain cell type developed at 108 months, which led to the patient's death. We conclude that there are two types of perianal Paget's disease. One type has endodermal differentiation with gastrointestinal-type glands containing intraluminal dirty necrosis, numerous signet ring cells, CK20 positivity, and GCDFP15 negativity. Such cases are especially likely to be associated with synchronous or metachronous rectal adenocarcinoma. The other type is a primary cutaneous intraepithelial neoplasm in which the Paget's cells display sweat gland differentiation, including GCDFP15 positivity; it generally lacks gastrointestinal-type glands, intraluminal dirty necrosis, and CK20 positivity. The CK7 is a sensitive, albeit nonspecific, marker for Paget's cells.
肛周佩吉特病较为罕见,其与相关区域内癌症的关系尚不明确。我们分析了11例肛周佩吉特病患者的组织学和免疫组化特征,以确定相关区域内癌的发生率及关系,并深入了解其组织发生情况。在5例确诊为直肠腺癌的患者中,4例是在佩吉特病同时发现的,1例是随后发现的。4例中印戒样佩吉特细胞占主导。4例出现上皮内腺体伴管腔内污秽坏死。在研究的4例中,上皮内佩吉特细胞和浸润性直肠腺癌的免疫表型均为细胞角蛋白(CK)7+/CK20+/大汗腺囊肿病液体蛋白-(GCDFP)。6例患者未确诊直肠腺癌。4例患者的佩吉特细胞为CK7+/CK20-/GCDFP15+。其中3例为单纯上皮内佩吉特病,广泛局部切除后均未发生浸润或转移。第4例患者出现双侧腹股沟淋巴结转移,在诊断佩吉特病8个月后死亡。2例患者佩吉特细胞为CK7+/CK20+/GCDFP15-。1例患者在7个月时出现复发性上皮内肛周佩吉特病;该患者在24个月时无病存活,另1例患者出现多次上皮内肛周佩吉特病复发,随后在108个月时出现一个细胞类型不明的巨大肛周肿瘤,导致患者死亡。我们得出结论,肛周佩吉特病有两种类型。一种类型具有内胚层分化,伴有含管腔内污秽坏死的胃肠型腺体、大量印戒细胞、CK20阳性和GCDFP15阴性。此类病例尤其可能与同时性或异时性直肠腺癌相关。另一种类型是原发性皮肤上皮内肿瘤,其中佩吉特细胞表现为汗腺分化,包括GCDFP15阳性;它通常缺乏胃肠型腺体、管腔内污秽坏死和CK20阳性。CK7是佩吉特细胞的一个敏感但非特异性的标志物。