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Pathologic Rupture of the Spleen in Mantle-Cell-Type Non-Hodgkin's Lymphoma
Christopher B Tan1, Dhyan Rajan, Sumreen Majeed
1Department of Internal Medicine, Nassau University Medical Center, East Meadow, NY 11554, USA.
Abstract:
Mantle cell lymphoma (MCL) accounts for less than 10 percent of all non-Hodgkin's lymphoma (NHL). Pathologic or spontaneous rupture of the spleen has been reported in patients with lymphoma; however only 5 cases have been reported in patients with MCL. Although splenomegaly occurs frequently in patients with MCL, spontaneous splenic rupture is rare. We present a case of a 51-year-old female with MCL, who presented to the medical emergency room with splenic rupture. This case illustrates that clinicians should be aware of the incidence and presentation of patients with MCL and spontaneous splenic rupture, as early detection and heightened suspicion may prevent potentially fatal outcomes.
Insights
Mantle cell lymphoma (MCL) rarely causes spontaneous splenic rupture. Early recognition in patients with MCL is crucial for prompt diagnosis and preventing fatal outcomes.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin's lymphoma (NHL).
- Splenomegaly is common in MCL, but splenic rupture is a rare complication.
- Only five cases of spontaneous splenic rupture in MCL patients have been previously reported.
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