1. A Rare Combination of Gastric Mucosa-associated Lymphoid Tissue Lymphoma, Autoimmune Gastritis, Thyroiditis, Hemolysis, and Systemic Lupus Erythematosus
- Author
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Takahiro Takemoto, Tohru Kotera, Shigemi Nakajima, Katsuhiko Itani, Kazue Ooyama, Hitoji Uchiyama, Shinsaku Imashuku, and Kuniaki Hirata
- Subjects
Anemia, Hemolytic ,Thyroiditis ,medicine.medical_specialty ,Autoimmune Gastritis ,Biopsy ,Case Report ,autoimmune gastritis ,030204 cardiovascular system & hematology ,Gastroenterology ,Endoscopy, Gastrointestinal ,Autoimmune Diseases ,Autoimmune thyroiditis ,03 medical and health sciences ,0302 clinical medicine ,systemic lupus erythematosus ,immune system diseases ,hemic and lymphatic diseases ,Internal medicine ,Internal Medicine ,medicine ,Humans ,Lupus Erythematosus, Systemic ,mucosa-associated lymphoid tissue lymphoma ,Systemic lupus erythematosus ,biology ,business.industry ,MALT lymphoma ,Lymphoma, B-Cell, Marginal Zone ,General Medicine ,Middle Aged ,Helicobacter pylori ,medicine.disease ,biology.organism_classification ,Lymphoma ,Gastric Mucosa ,Gastritis ,Female ,Radiography, Thoracic ,030211 gastroenterology & hepatology ,Autoimmune hemolytic anemia ,business - Abstract
We herein report a case with the rare combination of mucosa-associated lymphoid tissue lymphoma (MALT lymphoma) of the stomach, autoimmune gastritis (AIG), autoimmune thyroiditis, autoimmune hemolytic anemia (AIHA), and systemic lupus erythematosus. A 68-year-old woman was diagnosed with gastric MALT lymphoma associated with Helicobacter pylori (H. pylori) infection and AIG. Complete remission of the MALT lymphoma was achieved by H. pylori eradication and radiotherapy. Three years after the diagnosis of MALT lymphoma, the patient developed AIHA and anti-nuclear and anti-Smith autoantibody-positive lupus serositis, which were successfully managed with prednisolone administration.
- Published
- 2020
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