Extrapulmonary Small Cell Carcinoma Workup

  • Author: Irfan Maghfoor, MD; Chief Editor: Jules E Harris, MD   more...
 
Updated: Feb 28, 2012
 

Laboratory Studies

No laboratory investigations aid in the diagnosis of extrapulmonary small cell carcinoma. Most of the laboratory studies done in the workup are to assess end organ function prior to instituting therapy, especially chemotherapy, or to diagnose a suspected paraneoplastic syndrome.

  • Complete blood count with differential is obtained to assess bone marrow reserve, but it may give clues to bone marrow infiltration by the tumor. Bone marrow infiltration is suspected based on a leukoerythroblastic (presence of red and white blood cell precursors in peripheral blood) picture of peripheral blood.
  • Blood urea nitrogen and serum creatinine and electrolytes are obtained to asses renal function prior to instituting potentially nephrotoxic drugs as well as estimate renal clearance of chemotherapeutic agents. In addition, low sodium and abnormalities in other electrolytes such as potassium may point towards presence of a paraneoplastic syndrome.
  • Serum bilirubin and transaminases are obtained to assess liver function and for appropriate dosing of hepatically cleared chemotherapeutic agents.
  • Serum calcium is assessed for suspected hypercalcemia and bone metastases.
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Imaging Studies

The diagnosis of extrapulmonary small cell carcinoma by definition requires a chest radiograph, computed tomographic scan, or both without findings of chest involvement.

  • Chest radiograph is obtained to exclude pulmonary involvement.
  • CT scan of chest, abdomen, and pelvis is obtained to exclude pulmonary involvement and stage the extent of disease.
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Procedures

  • Bone marrow aspiration and biopsy are performed to confirm or rule out bone marrow involvement in case of peripheral blood abnormalities. Some authors recommend that bone marrow biopsy should be done in every patient to confirm limited disease.
  • Sputum cytology, bronchoscopy, or both are performed to exclude pulmonary origin of small cell carcinoma.
  • Special tests may be performed depending on primary site of origin:
    • Upper endoscopy: Esophagus
    • Direct laryngoscopy, bronchoscopy, and upper endoscopy: Origin in head and neck region
    • Cystoscopy: Urinary bladder
    • Lower endoscopy: Rectum and large bowel
    • Pelvic examination: Cervix and uterus
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Histologic Findings

Extrapulmonary small cell carcinoma histologically consists of sheets of uniform small round cells with scant cytoplasm, dense nuclei, and indistinct nucleoli.

Immunohistochemical stains with silver impregnated stains usually have positive results.

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Staging

There is no American Joint Committee on Cancer (AJCC) staging classification for extrapulmonary small cell carcinoma. In the reported literature, extrapulmonary small cell carcinoma is universally staged similarly to small cell carcinoma of lung, that is limited stage and extensive stage.

  • Limited stage: Tumor is confined to organ of origin with or without regional lymph node involvement. Alternatively, limited stage has also been defined as that encompassed within one radiation port.
  • Extensive stage: Disease has spread to distant organs or beyond regional lymph nodes.
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Contributor Information and Disclosures
Author

Irfan Maghfoor, MD  Consulting Oncologist, Department of Oncology, King Faisal Specialist Hospital and Research Center, Saudi Arabia

Irfan Maghfoor, MD is a member of the following medical societies: American Society of Hematology

Disclosure: Nothing to disclose.

Specialty Editor Board

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 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.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Rajalaxmi McKenna, MD, FACP  Southwest Medical Consultants, SC, Department of Medicine, 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  Clinical Professor of Medicine, Section of Hematology/Oncology, University of Arizona College of Medicine, 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 Society of Hematology, and Central Society for Clinical Research

Disclosure: GlobeImmune Salary Consulting

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