Al Hallak M N, Zouain N
University of North Dakota School of Medicine, MeritCare Health System, Roger Maris Cancer Center, Department of Radiation, Fargo, N. Dak., USA.
Case Rep Gastroenterol. 2009 Nov 20;3(3):332-337. doi: 10.1159/000256382.
Perianal Paget's disease is a rare malignancy. It is rarely isolated and often associated with an underlying adenocarcinoma. It usually presents with anal itchiness and discomfort and can be misdiagnosed as hemorrhoids. Once the diagnosis of perianal Paget's disease is granted, extensive work-up to find an underlying primary malignancy is crucial. Surgery is the standard modality of treatment of extramammary Paget's disease (EMPD) with recurrence rates of 44-60%. Other different treatment modalities including radiotherapy, laser therapy, topical and systemic chemotherapy and the new emerging, promising photodynamic therapy are in the field of study. A 76-year-old man was referred to our hospital with a one-year history of anal itchiness and intermittent rectal bleeding. Skin shave and punch biopsies from the perianal area were reported back as perianal Paget's disease with no underlying adenocarcinoma. The immunohistochemical stains were positive for cytokeratin 7 but also positive for cytokeratin 20 and CEA which indicated the essentiality of extensive investigations to find a primary malignancy. Skin exam showed no primary source. The investigations were unable to find the primary malignancy. Given the results of immunohistochemical stains we recommended local perianal Paget's disease resection. The intraoperative frozen section showed adenocarcinoma around the anal sphincter. Ten days later the patient underwent an abdominoperineal resection and the final pathology report showed extensive adenocarcinoma in three quadrants of the perianal area with focal involvement of the rectal mucosa. We recommended an adjuvant chemotherapy with FOLFOX following surgery given the bulkiness of the disease. We conclude that once perianal Paget's disease is diagnosed, an extensive work-up should be done to find the underlying primary malignancy. Immunohistochemical stains are helpful in raising the suspicion of underlying primary malignancy. Finding an underlying primary malignancy in patients with EMPD is prompt to choose the treatment modality and estimate the prognosis.
肛周佩吉特病是一种罕见的恶性肿瘤。它很少单独出现,常与潜在的腺癌相关。其通常表现为肛门瘙痒和不适,可能被误诊为痔疮。一旦确诊为肛周佩吉特病,进行全面检查以发现潜在的原发性恶性肿瘤至关重要。手术是治疗乳腺外佩吉特病(EMPD)的标准方式,复发率为44% - 60%。其他不同的治疗方式,包括放疗、激光治疗、局部和全身化疗以及新兴且有前景的光动力疗法,都在研究领域。一名76岁男性因有一年肛门瘙痒和间歇性直肠出血病史被转诊至我院。肛周区域的皮肤削除活检和打孔活检报告为肛周佩吉特病,未发现潜在腺癌。免疫组化染色细胞角蛋白7呈阳性,但细胞角蛋白20和癌胚抗原也呈阳性,这表明进行全面检查以发现原发性恶性肿瘤的必要性。皮肤检查未发现原发灶。各项检查未能找到原发性恶性肿瘤。鉴于免疫组化染色结果,我们建议行局部肛周佩吉特病切除术。术中冰冻切片显示肛门括约肌周围有腺癌。十天后患者接受了腹会阴联合切除术,最终病理报告显示肛周区域三个象限有广泛腺癌,直肠黏膜有局灶性受累。鉴于疾病范围较大,我们建议术后采用FOLFOX辅助化疗。我们得出结论,一旦诊断为肛周佩吉特病,应进行全面检查以发现潜在的原发性恶性肿瘤。免疫组化染色有助于提高对潜在原发性恶性肿瘤的怀疑。在EMPD患者中发现潜在的原发性恶性肿瘤有助于选择治疗方式并评估预后。