Asymptomatic Multiple Lymphomatous Polyposis Identified during Staging Bidirectional Endoscopy of Mantle Cell Lymphoma
Autor: | Frances J. Jones, Alexander W. Brown, Sonja P. Dawsey, Jason A. Gregory |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Pathology medicine.medical_specialty Leptomeningeal Multiple Lymphomatous Polyposis Case Report Asymptomatic lcsh:RC254-282 03 medical and health sciences 0302 clinical medicine medicine Gastrointestinal tract Mantle cell lymphoma medicine.diagnostic_test business.industry Multiple lymphomatous polyposis Endoscopy medicine.disease lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens Gastrointestinal neoplasms 030104 developmental biology Oncology 030220 oncology & carcinogenesis medicine.symptom business |
Zdroj: | Case Reports in Oncology, Vol 9, Iss 3, Pp 661-665 (2016) Case Reports in Oncology |
ISSN: | 1662-6575 |
Popis: | Multiple lymphomatous polyposis (MLP) as an extranodal manifestation of mantle cell lymphoma (MCL) in the gastrointestinal tract is rare and not often reported in the literature. We describe the case of a 63-year-old female with asymptomatic MLP found during staging bidirectional endoscopy of MCL. The patient presented only with dyspnea, but was found on physical exam to have diffuse lymphadenopathy, and subsequent positron emission tomography (PET) CT showed extensive lymph node adenopathy consistent with lymphoma. Excisional lymph node biopsy revealed high-risk MCL. Prior to therapy, staging bidirectional endoscopy was performed, which revealed duodenal bulb polyps and diffuse polyposis in the colon. Biopsies showed atypical lymphoid infiltrate identical to the initial excisional lymph node biopsy. The patient underwent aggressive induction therapy, chemotherapy and bone marrow transplantation. Four months later, repeat colonoscopy and biopsies showed normal mucosa, and repeat PET CT showed no evidence of systemic disease. Eight months later, the patient began having symptoms consistent with cauda equina syndrome, and she was found to have leptomeningeal recurrence of MCL. In spite of other medical treatment, the patient’s MCL progressed and she passed away 3 years after the initial presentation. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |