- Case report
- Open Access
- Open Peer Review
Immunohistochemical identification of primary peritoneal serous cystadenocarcinoma mimicking advanced colorectal carcinoma: a case report
© von Riedenauer et al; licensee BioMed Central Ltd. 2007
- Received: 24 June 2007
- Accepted: 26 November 2007
- Published: 26 November 2007
Primary peritoneal cystadenocarcinoma is a rare tumor of similar histogenic origin as primary ovarian carcinoma. We present a case of primary peritoneal serous cystadenocarcinoma mimicking advanced colorectal cancer in a 68 yr-old African American female. Radiology, endoscopy and cytology yielded only inconclusive findings. Immunohistochemical analysis of percutaneously obtained ascitic fluid provided a correct diagnosis of primary peritoneal cystadenocarcinoma. The discovery of serous ascites at the time of laparotomy confirmed a diagnosis of primary peritoneal serous cystadenocarcinoma. Final surgical pathology reconfirmed the diagnosis of primary peritoneal cystadenocarcinoma. This case demonstrates the utility of immunohistochemistry for accurately diagnosing patients with inconclusive findings in the setting of peritoneal carcinomatosis and primary peritoneal cystadenocarcinoma.
- Estrogen Receptor
- Ovarian Carcinoma
- Peritoneal Carcinomatosis
- Advanced Colorectal Cancer
Primary peritoneal cystadenocarcinoma is a rare tumor . Originally described by Swerdlow in 1959, the true incidence of primary peritoneal cystadenocarcinoma remains unknown although an estimated relative frequency to ovarian cancer is 1:10. Better recognition of this entity in recent years has contributed to an increasing diagnostic frequency approaching 18% of laparotomies performed for ovarian carcinoma . Synonyms for primary peritoneal cystadenocarcinoma include primary peritoneal papillary carcinoma, extraovarian peritoneal papillary carcinoma, peritoneal mesothelioma, surface papillary carcinoma, primary peritoneal carcinoma, and multiple focal extraovarian carcinoma . Primary ovarian carcinoma may present as a solitary mass, but is the most common cause of carcinomatosis in women. Primary peritoneal cystadenocarcinoma uniformly presents as disseminated intraperitoneal carcinomatosis.
Both primary ovarian carcinoma and primary peritoneal cystadenocarcinoma can present with carcinomatosis. Clinical presentation results from local tumor effects involving multiple organs . Common symptoms include abdominal distension/ascites, dyspnea, nausea, vomiting and constipation. The most common presenting complaints are ascites, abdominal mass and pleural effusion. Both primary ovarian carcinoma and primary peritoneal cystadenocarcinoma have serous and mucinous subtypes. The serous subtypes, primary serous ovarian carcinoma and primary peritoneal serous cystadenocarcinoma, predominate over the mucinous subtypes in both primary ovarian carcinoma and primary peritoneal cystadenocarcinoma. Ascites and abdominal distension appear more frequently with primary peritoneal cystadenocarcinoma than with primary ovarian carcinoma. Primary ovarian carcinoma alternately presents more often with a palpable pelvic mass. Primary peritoneal cystadenocarcinoma and primary ovarian carcinoma are immunohistochemically indistinguishable [1, 4]. Both malignancies stain positive for CK7, ER, Mesothelin and CA125. Primary peritoneal cystadenocarcinoma is histologically distinguished from primary ovarian carcinoma by ovaries of normal size or enlarged secondary to a benign process, extraovarian involvement greater than ovarian involvement, and ovarian surface penetration of less than 5 mm depth [1, 3, 4].
Management of primary peritoneal cystadenocarcinoma has followed treatment of primary ovarian carcinoma with surgical debulking and adjuvant platinum-containing chemotherapy . Survival in primary peritoneal serous cystadenocarcinoma parallels survival of stage III–IV primary serous ovarian carcinoma [1, 4, 5]. Median survivals for primary peritoneal serous cystadenocarcinoma and primary serous ovarian carcinoma are equivalent and range from 32–40 months [1, 5].
Primary peritoneal cystadenocarcinoma and primary ovarian carcinoma both stain positive for estrogen receptor (ER), cytokeratin 7 (CK7), Wilm's tumor suppressor gene (WT1), and cancer antigen 125 (CA 125). Neither entity possesses cytokeratin 20 (CK 20), progesterone receptor (PR), Calretinin, carcinoembryonic antigen (CEA), gross cystic disease fluid protein (BRST-2), and thyroid transcription factor 1 (TTF1). Cytochemical overlap can occur between different celltypes but the constellation of positive and negative antigenicity produces a unique immunohistochemical "fingerprint" that identifies cellular origin.
The patient presented with a diagnosis of metastatic adenocarcinoma of the colon. Her personal history of colonic polyps and her strong family history of colon cancer supported this diagnosis. Endoscopic and pathologic findings were inconsistent with advanced colorectal cancer. Radiologic imaging demonstrated peritoneal carcinomatosis but could not identify a unique origin. Accurately identifying the origin of the patient's peritoneal carcinomatosis predicated appropriate therapy as treatment differs among the varying malignancies causing peritoneal carcinomatosis. Disease progression and survival also differ among the varying malignancies causing peritoneal carcinomatosis and correct identification of malignant origin was required for accurate prognosis.
Breast and gastrointestinal metastasis may clinically, radiologically and biochemically mimic primary ovarian and primary peritoneal adenocarcinoma . Peritoneal mesothelioma and pulmonary malignancies can also present clinically similar to primary ovarian carcinoma and primary peritoneal cystadenocarcinoma with abdominal pain and ascitic distension. Treatment of primary peritoneal mesothelioma and carcinomatosis from metastatic breast, lung and gastrointestinal cancers differ significantly from the treatment of primary ovarian and primary peritoneal adenocarcinoma. Surgical debulking with intraoperative hyperthermic chemotherapy provides some survival advantage with peritoneal mesothelioma . Advanced peritoneal mesothelioma is treated with combination systemic chemotherapy . Overall survival with peritoneal mesothelioma is less than twelve months . Peritoneal carcinomatosis resulting from colorectal primaries has also been treated with intraoperative hyperthermic chemotherapy an surgical debulking . Survival in patients with peritoneal carcinomatosis from colorectal primaries varies from 5.3 to 12.6 month . Systemic chemotherapy for peritoneal carcinomatosis resulting from advanced colorectal cancer is 5-fluorouracil (5-FU) based with the addition of Oxaliplatin, Irinotecan, Bevacizumab, and Cetuximab based on the patient's performance status and whether prior chemotherapy was provided . Median survival for peritoneal carcinomatosis secondary to disseminated pulmonary malignancies is 2 months . Surgical intervention with breast cancer carcinomatosis shows a variable survival advantage . Chemotherapy and hormonal manipulation prolongs survival with breast cancer carcinomatosis . Cytoreductive surgery combined with systemic cisplatin-based multiagent chemotherapy extends survival in both primary ovarian and primary peritoneal cystadenocarcinoma . Survival with carcinomatosis secondary to primary ovarian carcinoma and primary peritoneal cystadenocarcinoma can extend beyond thirty months .
Metastatic lung cancer and peritoneal mesothelioma were excluded based on the absence of pulmonary disease on radiologic imaging and the absence of characteristic histopathologic features on biopsy, respectively. The patient reported a personal history of breast cancer, ductal carcinoma in situ, treated with lumpectomy and radiation therapy five years prior. Surgical margins were negative. Tamoxifen was prescribed following completion of her radiation therapy, but was discontinued after one month. This history of breast cancer raised our suspicion of a breast origin. Metastatic breast cancer was considered unlikely given the rarity of peritoneal carcinomatosis from this disease in the absence of any other evidence of metastasis. Primary ovarian carcinoma was considered given the patient's personal history of breast cancer. Genetic testing was not performed. Consultation with the gynecologic oncology service disavowed a primary ovarian etiology. The possibility of primary peritoneal adenocarcinoma became prescient.
Immunohistochemical analysis lead to the correct identification of primary peritoneal cystadenocarcinoma while excluding alternate diagnoses. Tumor markers ordered included: CK7, CK20, TTF1, ER, PR, Calretinin, WT1, CA 125, BRST-2, and CEA. Colon adenocarcinoma stains positive for CK20 and typically negative for CK7, CA125, TTF1 and ER. Breast cancer cells typically stain positive for CK7, ER and are negative for CA125, CK20, and TTF1. Ovarian carcinoma binds antigens for CK7, CA125, ER, and is negative for CDX2, CK20, and TTF1. The patient's cells were immunohistochemically negative for CK20, TTF1, Calretinin, PR and BRST-2. Her immunohistochemistry was positive for CA125, WT1, CK7, and ER. Primary peritoneal cystadenocarcinoma bears antigens CK7, ER, WT1, and CA125. The constellation of symptoms, endoscopic morphology, imaging results, histo-pathologic and immunohistochemical findings portrayed primary peritoneal cystadenocarcinoma. Immunohistochemistry allowed the patient to be diagnosed without surgery. Without immunohistochemical technology, patients with diagnostically uncertain peritoneal carcinomatosis formerly required open or laparoscopic tissue biopsy with further operative interventions pending histologic analysis. Immunohistochemistry facilitated diagnosis without surgery.
Preoperatively discerning primary peritoneal serous cystadenocarcinoma from primary peritoneal mucinous adenocarcinoma was not possible as these two entities are indistinguishable immunohistochemically and histologically. Primary peritoneal serous cystadenocarcinoma was confirmed by the intraoperative finding of clear ascites and the patient was afforded significant tumor debulking. Histo-pathology returned a diagnosis of moderately differentiated invasive papillary adenocarcinoma, which was consistent with primary peritoneal cystadenocarcinoma. Our institution does not offer surgical debulking for peritoneal carcinomatosis secondary to advanced colorectal cancer. Persistent misdiagnosis of advanced colorectal cancer would have then resulted in suboptimal treatment of this patient by forgoing surgical debulking and assigning inappropriate chemotherapy.
Cognizance of primary peritoneal cystadenocarcinoma and the utility of immunohistochemistry permitted the accurate diagnosis of a patient previously misidentified as having advanced colorectal adenocarcinoma. Correctly diagnosing primary peritoneal cystadenocarcinoma dramatically affected this patient's prognosis as opposed to metastatic colorectal adenocarcinoma with carcinomatosis. The incidence of primary peritoneal cystadenocarcinoma has increased dramatically over the past 10 years . Perhaps the incident rise in primary peritoneal cystadenocarcinoma has resulted from a rising awareness of this disease and an increased ability to pathologically distinguish this disease. With the known ability of gastrointestinal malignancies to mimic gynecologic cancer, and with 1.1% of cancers referred to gynecologic oncologists reported to be nongynecologic , the ability to distinguish advanced colorectal cancer from primary peritoneal cystadenocarcinoma and primary ovarian carcinoma has become more important. Immunohistochemical technology demonstrated marked utility for distinguishing primary peritoneal cystadenocarcinoma from other mimicking diseases in the setting of unknown primary peritoneal carcinomatosis. This technology was successful using only paracentesis and thus obviated the risks and morbidity of surgical biopsy. Immunohistochemistry facilitated preoperative diagnostic certainty and thereby improved surgical planning. Improved patient outcomes may result from further use of immunohistochemical analysis to diagnose unknown primary peritoneal carcinomatosis.
Written informed consent was obtained from the patient for publication of the study.
No sources of funding were involved in the production of this manuscript or the conduct of this study.
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