A 62-year-old man was referred because of intestinal polyposis. Physical examination
revealed diffuse lymphadenopathy and splenomegaly. Laboratory tests showed lactate
dehydrogenase of 173 U/L (reference range [RR] 120-250 U/L) and soluble interleukin-2
receptor of 3264 U/mL (RR 220-530 U/mL). Colonoscopy revealed multiple smooth polyps
(<10 mm) in the terminal ileum and colon. EGD to determine the extent of the disease
revealed multiple whitish flat nodules (<5 mm) in the pharynx and esophagus by white
light (A) and narrow-band imaging (B). Magnifying endoscopy with narrow-band imaging showed smooth lesions with treelike
abnormal vessels (C). None of the lesions stained with Lugol iodine solution. Histologic examination
of biopsy specimens from the pharynx, esophagus, and colon showed nodular aggregates
of small lymphocytes in the subepithelium. Immunohistochemical studies revealed expression
of CD20, CD5, and cyclin D1 (D, cyclin D1, orig. mag. ×100). The proliferative index assessed by Ki-67 was 40%. 18F-fluorodeoxyglucose positron
emission tomography revealed abnormal uptake in the spleen, colon, and lymph nodes
on both sides of the diaphragm. The result of pathologic examination of the bone marrow
was normal. Thus, the patient received a diagnosis of stage IV mantle cell lymphoma
(Lugano classification). The patient underwent chemotherapy, which resulted in obvious
shrinking of the lesions in the digestive tract and lymph nodes.
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Publication history
Published online: July 15, 2017
Massimo Raimondo, MD, Associate Editor for Focal PointsIdentification
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© 2018 by the American Society for Gastrointestinal Endoscopy