1.A Case of Primary Esophageal B-cell Lymphoma of MALT type, Presenting as a Submucosal Tumor.
Chan Sup SHIM ; Joon Seong LEE ; Jin Oh KIM ; Joo Young CHO ; Moon Sung LEE ; So Young JIN ; Wook YOUM
Journal of Korean Medical Science 2003;18(1):120-124
The primary esophageal lymphoma is extremely rare, and shows various morphologic characteristics. Only a single case of mucosa-associated lymphoid tissue (MALT) type lymphoma confined to the esophagus has been reported in the literature. A 61-yr-old man was referred to our hospital for evaluation of an esophageal submucosal tumor (SMT) that had been detected incidentally by endoscopy. He had a history of pulmonary tuberculosis with long-term anti-tuberculosis medication 15 yr before, and also had a history of syphilis, which had been treated one year before. He had been taking a synthetic thyroid hormones for the past 10 months because of an autoimmune thyroiditis. Endoscopy showed a longitudinal round and tubular shaped smooth elevated lesion, which was covered with intact mucosa and located at the mid to distal esophagus, 31 cm to 39 cm from the incisor teeth. Endoscopic ultrasonography (EUS) showed a huge longitudinal growing intermediate- to hypo-echoic mass located in the submucosal layer with internal small, various sized honeycomb-like anechoic lesions suggesting germinal centers. Subsequently, he underwent a surgery, which confirmed the mass as a primary esophageal low-grade B-cell lymphoma of MALT type.
Alcoholism/complications
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Diagnosis, Differential
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Esophageal Neoplasms/pathology*
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Esophageal Neoplasms/radiography
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Esophageal Neoplasms/ultrasonography
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Esophagoscopy
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Gastritis/complications
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Helicobacter Infections/complications
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Hemangioma, Cavernous/diagnosis
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Human
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Incidental Findings
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Lymphoma, Mucosa-Associated Lymphoid Tissue/pathology*
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Lymphoma, Mucosa-Associated Lymphoid Tissue/radiography
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Lymphoma, Mucosa-Associated Lymphoid Tissue/ultrasonography
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Male
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Middle Aged
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Mucous Membrane/pathology
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Neoplasm Invasiveness
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Smoking
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Thyroiditis, Autoimmune/complications
2.Thyrotoxic Periodic Paralysis Associated with Transient Thyrotoxicosis Due to Painless Thyroiditis.
Sang Bo OH ; Jinhee AHN ; Min Young OH ; Bo Gwang CHOI ; Ji Hyun KANG ; Yun Kyung JEON ; Sang Soo KIM ; Bo Hyun KIM ; Yong Ki KIM ; In Joo KIM
Journal of Korean Medical Science 2012;27(7):822-826
Thyrotoxic periodic paralysis (TPP) is a rare manifestation of hyperthyroidism characterized by muscle weakness and hypokalemia. All ethnicities can be affected, but TPP typically presents in men of Asian descent. The most common cause of TPP in thyrotoxicosis is Graves' disease. However, TPP can occur with any form of thyrotoxicosis. Up to our knowledge, very few cases ever reported the relationship between TPP and painless thyroiditis. We herein report a 25-yr-old Korean man who suffered from flaccid paralysis of the lower extremities and numbness of hands. The patient was subsequently diagnosed as having TPP associated with transient thyrotoxicosis due to painless thyroiditis. The paralytic attack did not recur after improving the thyroid function. Therefore, it is necessary that early diagnosis of TPP due to transient thyrotoxicosis is made to administer definite treatment and prevent recurrent paralysis.
Administration, Oral
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Adult
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Anti-Arrhythmia Agents/therapeutic use
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Humans
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Hypokalemic Periodic Paralysis/*diagnosis/drug therapy/etiology
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Male
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Organotechnetium Compounds/chemistry/diagnostic use
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Potassium Chloride/therapeutic use
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Propranolol/therapeutic use
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Radiopharmaceuticals/diagnostic use
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Thyroiditis/*complications/radiography/ultrasonography
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Thyrotoxicosis/*diagnosis/etiology