eMedicine Specialties > Oncology > Carcinomas of the Gastrointestinal Tract

Peritoneal Cancer: Differential Diagnoses & Workup

Author: Wissam Bleibel, MD, Staff Physician, Department of Internal Medicine, Caritas Carney Hospital, Tufts University School of Medicine
Coauthor(s): Olga Kozyreva, MD, Fellow, Department of Hematology-Oncology, Tufts University School of Medicine; Sarah K May, MD, Consulting Staff, Department of Hematology-Oncology, Caritas Carney Hospital, Commonwealth Hematology-Oncology PC; Daniel Efiom-Ekaha, MD, Fellow in Hematology/Oncology, Department of Internal Medicine, State University of New York-Downstate; Arunbhai G Patel, MD, Chief, Department of Internal Medicine, Division of Hematology-Oncology, Brooklyn Hospital Center; Adekunle Kuku, MD, Staff Physician, Department of Internal Medicine, Brooklyn Hospital Center
Contributor Information and Disclosures

Updated: Jul 23, 2007

Differential Diagnoses

Ovarian Cysts

Other Problems to Be Considered

The differential diagnosis of primary peritoneal cancers includes peritoneal metastasis (ie, peritoneal carcinomatosis) from primary sites including the GI tract, ovaries, or breast or as part of the syndrome of adenocarcinomas of unknown primary site. Although the primary histology findings dictate the clinical course, important concepts of diagnosis and treatment are common to all forms. The most important risk factor for developing peritoneal carcinomatosis is the depth of invasion of the primary tumor.

Reactive tumorlike lesions of the peritoneum have been described and should be included in the differential diagnosis of primary peritoneal cancers, as follows:

  • Granulomatous lesions
    • Vernix caseosa and meconium peritonitis
    • Granulomatous peritonitis secondary to foreign material, including keratin
    • Necrotic pseudoxanthomatous nodules
    • Postcautery granulomas
  • Nongranulomatous histiocytic lesions
    • Ceroid-rich histiocytic infiltrates
    • Peritoneal melanosis
    • Mucicarminophilic histiocytosis
    • Other histiocytic infiltrates
  • Fibrosing lesions
    • Sclerosing peritonitis
    • Peritoneal fibrosis nodules
  • Mesothelial lesions
    • Mesothelial hyperplasia
    • Peritoneal inclusion cysts
Pseudomyxoma peritonei typically includes any low-grade or benign tumor within the abdominal cavity that produces copious amounts of mucinous ascites. This condition includes peritoneal spread from well-differentiated adenocarcinomas of the GI tract and benign mucin-secreting adenomas of the appendix.

Workup

Laboratory Studies

Malignant peritoneal mesothelioma: Findings from cytologic examination of ascites can suggest the diagnosis, and findings from percutaneous biopsy of the omentum can help verify the diagnosis. This condition is usually confined to the abdomen at the time of diagnosis.

Imaging Studies

  • Standard imaging tests, including ultrasonography and helical CT scans, are notably insensitive for the detection of peritoneal tumors.
    • The sensitivity of CT scans for peritoneal nodules measuring smaller than 1 cm is approximately 15-30%.
    • Ultrasonography is similarly insensitive; therefore, considering findings, rather than solid tumor detection, that may suggest the presence of peritoneal lesions is important. These include the presence of ascites, fixing together of bowel loops, thickening of mesentery, and omental matting.
  • CT scan findings are nonspecific in primary papillary serous carcinoma of the peritoneum. Consider this diagnosis when findings include ascites, omental caking, and diffuse enhancement with nodular thickening of the parietal peritoneum of the pelvis observed with normal-sized ovaries, with or without a fine enhancing surface nodularity of the ovary.
  • Some studies show that MRI is superior to helical CT scan for the detection of peritoneal and bowel wall abnormalities.
  • Positron emission tomography imaging has not been shown to be sensitive for lesions smaller than 1 cm in the abdominal cavity.
  • Findings from radionuclide scan studies can help confirm the diagnosis of peritoneal hemangiomas; the isotope concentrates in the area where platelets are being sequestered. A CT scan and ultrasound also may detect larger hemangiomas. Angiographic evaluation is a more precise, although invasive, procedure when radionuclide scans, CT scan, and ultrasound findings are negative.

Procedures

  • Procedures for the workup of peritoneal lesions include peritoneal lavage cytology. This can be performed using a cutaneous closed technique or at the time of laparoscopy or laparotomy. The sensitivity of the test results depends on the ability to completely lavage all regions of the peritoneal cavity and the ability to detect cancer cells being shed into the peritoneal cavity by the tumor.
  • Direct visualization of the peritoneal surfaces along with palpation of the abdominal contents is by far the most sensitive modality for detecting peritoneal cancer. This can be accomplished with a minimally invasive approach (ie, laparoscopy), which allows for safe, directed peritoneal lavage for cytology and with open abdominal exploration and palpation of the peritoneal surfaces. Open abdominal exploration and palpation are extremely sensitive for 1- to 2-mm peritoneal nodules.

Histologic Findings

Primary peritoneal carcinoma is histologically indistinguishable from primary epithelial ovarian carcinoma; however, primary ovarian cancer can be excluded based on certain criteria. First, both ovaries must be of normal in size. Second, the extraovarian involvement must be greater than the involvement on the surface of the ovary. Third, the ovarian component must be smaller than 5 by 5 mm within the ovary or confined to the ovarian surface. Finally, the cytologic characteristics must be of the serous type.

More on Peritoneal Cancer

Overview: Peritoneal Cancer
Differential Diagnoses & Workup: Peritoneal Cancer
Treatment & Medication: Peritoneal Cancer
Follow-up: Peritoneal Cancer
References

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Further Reading

Keywords

ovarian cancer, malignant mesothelioma, benign papillary mesothelioma, desmoplastic small round cell tumors, DSRCT, peritoneal angiosarcoma, leiomyomatosis peritonealis disseminata, LPD, peritoneal hemangiomatosis, primary peritoneal cancer, peritoneal malignancy, peritoneum, peritoneal carcinoma, peritoneal carcinoma, abdominal therapeutic radiation, radiation therapy, asbestos exposure, cystic mesothelioma, multilocular peritoneal inclusion cyst, primary peritoneal carcinoma, serous surface papillary carcinoma

Contributor Information and Disclosures

Author

Wissam Bleibel, MD, Staff Physician, Department of Internal Medicine, Caritas Carney Hospital, Tufts University School of Medicine
Wissam Bleibel, MD is a member of the following medical societies: American Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Olga Kozyreva, MD, Fellow, Department of Hematology-Oncology, Tufts University School of Medicine
Disclosure: Nothing to disclose.

Sarah K May, MD, Consulting Staff, Department of Hematology-Oncology, Caritas Carney Hospital, Commonwealth Hematology-Oncology PC
Sarah K May, MD is a member of the following medical societies: American Society of Clinical Oncology
Disclosure: Nothing to disclose.

Daniel Efiom-Ekaha, MD, Fellow in Hematology/Oncology, Department of Internal Medicine, State University of New York-Downstate
Daniel Efiom-Ekaha, MD is a member of the following medical societies: American Medical Association
Disclosure: Nothing to disclose.

Arunbhai G Patel, MD, Chief, Department of Internal Medicine, Division of Hematology-Oncology, Brooklyn Hospital Center
Arunbhai G Patel, MD is a member of the following medical societies: American Medical Association
Disclosure: Nothing to disclose.

Adekunle Kuku, MD, Staff Physician, Department of Internal Medicine, Brooklyn Hospital Center
Disclosure: Nothing to disclose.

Medical Editor

Robert C Shepard, MD, FACP, Associate Professor of Medicine in Hematology and Oncology at University of North Carolina at Chapel Hill; Vice President of Scientific Affairs, Therapeutic Expertise, Oncology, at PRA International
Robert C Shepard, MD, FACP is a member of the following medical societies: American Association for Cancer Research, American College of Physician Executives, American College of Physicians, American Federation for Clinical Research, American Federation for Medical Research, American Medical Association, American Medical Informatics Association, American Society of Clinical Oncology, American Society of Hematology, Association of Clinical Research Professionals, Eastern Cooperative Oncology Group, European Society for Medical Oncology, Massachusetts Medical Society, and Society for Biological Therapy
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Benjamin Movsas, MD, Vice-Chairman, Department of Radiation Oncology, Fox Chase Cancer Center
Benjamin Movsas, MD is a member of the following medical societies: American College of Radiology, American Radium Society, American Society for Therapeutic Radiology and Oncology, and American Society of Clinical Oncology
Disclosure: Nothing to disclose.

CME Editor

Rajalaxmi McKenna, MD, FACP, Consulting Staff, Department of Medicine, Southwest Medical Consultants, SC, Good Samaritan Hospital, Advocate Health Systems
Rajalaxmi McKenna, MD, FACP is a member of the following medical societies: American Society of Clinical Oncology, American Society of Hematology, and International Society on Thrombosis and Haemostasis
Disclosure: Nothing to disclose.

Chief Editor

Jules E Harris, MD, Visiting Professor of Medicine, Division of Hematology/Medical Oncology, Department of Internal Medicine, University of Arizona College of Medicine at Tucson; Consulting Staff, Arizona Cancer Center
Jules E Harris, MD is a member of the following medical societies: American Association for Cancer Research, American Association for the Advancement of Science, American Association of Immunologists, American Federation for Clinical Research, American Society of Clinical Oncology, American Society of Hematology, Central Society for Clinical Research, Society for Biological Therapy, and Society for Leukocyte Biology
Disclosure: GlobeImmune Salary Consulting; Amplimed Consulting fee Consulting

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