Metastatic Hepatobiliary Cystadenocarcinoma Mimicking a Gynecologic Malignancy

IF 0.1 Q4 PATHOLOGY AJSP: reviews & reports Pub Date : 2022-01-01 DOI:10.1097/PCR.0000000000000460
E. O'Donnell, Kalpana M. Devaraj, M. Post
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Abstract

Abstract Hepatobiliary cystadenocarcinoma is a rare malignancy associated with ovarian-like stroma and overtly malignant glands that has a favorable prognosis if completely resected, analogous to minimally invasive adenocarcinoma arising in mucinous cystic neoplasms of the pancreas. Ovarian mucinous neoplasms may have a similar histologic appearance and are known to occasionally contain mural nodules of anaplastic carcinoma. We report a case of hepatobiliary cystadenocarcinoma that subsequently presented as metastatic disease mimicking a primary gynecological malignancy. The 30-year-old patient had a history of a completely resected hepatobiliary cystadenocarcinoma 2 years prior to presentation, without adjuvant therapy. She presented to her gynecologist with pelvic pain and vaginal bleeding. Physical examination revealed diffuse nodularity along the anterior vaginal wall, and imaging showed a 5.8 × 4.1 cm pelvic mass with diffuse metastatic disease. Biopsies of the vaginal wall and an inguinal lymph node showed nests of pleomorphic cells with squamoid and glandular features concerning for metastatic ovarian carcinoma; however, immunohistochemistry was negative for PAX8 and ER, but positive for CDX2. Subsequent review of the patient's prior resection revealed a cystic mucinous neoplasm with mural nodules of adenosquamous and anaplastic carcinoma, the latter previously reported only rarely in hepatobiliary cystadenocarcinoma. This case highlights the histologic overlap between hepatobiliary and ovarian neoplasms, which may present a diagnostic challenge, particularly in the setting of incomplete history. In addition, the unusual presence of an anaplastic component in the patient's original tumor portends a worse prognosis; therefore, additional therapy should be considered in these patients.
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模拟妇科恶性肿瘤的转移性肝胆囊腺癌
肝胆囊腺癌是一种罕见的与卵巢样间质和明显恶性腺体相关的恶性肿瘤,如果完全切除,预后良好,类似于胰腺粘液囊性肿瘤中出现的微创腺癌。卵巢黏液性肿瘤可能具有类似的组织学外观,并且已知偶尔包含间变性癌的壁结节。我们报告一例肝胆囊腺癌,随后表现为转移性疾病,模仿原发性妇科恶性肿瘤。30岁的患者在发病前2年有完全切除的肝胆囊腺癌病史,未接受辅助治疗。她向妇科医生提出盆腔疼痛和阴道出血。体格检查示阴道前壁弥漫性结节,影像学示5.8 × 4.1 cm盆腔肿块伴弥漫性转移。阴道壁和腹股沟淋巴结活检显示具有鳞状和腺状特征的多形性细胞巢,与转移性卵巢癌有关;PAX8、ER免疫组化阴性,CDX2免疫组化阳性。随后对患者先前切除的复查显示为囊性黏液肿瘤伴腺鳞癌和间变性癌的壁结节,后者以前仅在肝胆囊腺癌中罕见报道。该病例突出了肝胆和卵巢肿瘤的组织学重叠,这可能对诊断提出挑战,特别是在病史不完整的情况下。此外,患者原发肿瘤中不寻常的间变性成分预示着较差的预后;因此,这些患者应考虑额外的治疗。
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