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JYMS : Journal of Yeungnam Medical Science

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Tae Nyun Kim 3 Articles
A Case of Esophageal Bullous Pemphigoid Manifestated by Upper Gastrointestinal Bleeding
Kyeong Ok Kim, Byung Ik Jang, Jong Ryul Eun, Tae Nyun Kim
Yeungnam Univ J Med. 2007;24(2 Suppl):S671-675.   Published online December 31, 2007
DOI: https://doi.org/10.12701/yujm.2007.24.2S.S671
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  • 1 Crossref
AbstractAbstract PDF
Bullous pemphiogid (BP) is a chronic vesicular disorder and an autoimmune disease which has an autoantibodies to hemidesmosime in the keratinocyte. The authors report a case of gastrointestinal bleeding caused by BP involved with esophagus. A seventy year old man visited our clinic due to melena for a week. He had a quadriplegia due to fracture of cervical spine and was on therapy with corticosteroid and immunomodulatory drug for the diagnosis of BP. On endoscopic examination, multiple bullae filled with blood at lower esophagus was revealed and there was no other bleeding focus in stomach and duodenum. Medical treatment for BP with supportive care was done. The patient died due to sepsis caused by pneumonia. BP is common in elderly or poor conditioned patients. We need to consider the invasion of esophagus in case of gastrointestinal bleeding in patients with BP.

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Citations to this article as recorded by  
  • Esophageal Involvement of Bullous Pemphigoid
    Junseak Lee, Sanggon Moon, Chul-Hyun Lim
    The Korean Journal of Gastroenterology.2021; 78(4): 249.     CrossRef
A Case of Parathyroid Carcinoma with Systemic Calcification.
Heui Sik Kim, Chan Woo Lee, Sang Yiup Nam, Jin Chul Park, Ji Sang Yoon, Jae Chun Lee, Kyu Chang Won, Ihn Ho Cho, Tae Nyun Kim, Hyoung Woo Lee, Myung Soo Hyun, Hyun Woo Lee
Yeungnam Univ J Med. 1997;14(2):459-466.   Published online December 31, 1997
DOI: https://doi.org/10.12701/yujm.1997.14.2.459
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  • 1 Crossref
AbstractAbstract PDF
Hyperparathyroidism due to parathyroid cancer is rare. It is difficult to diagnose preoperatively but there should be an increased index of suspicion in those parathyroid Patient with palpable neck masses, profound hypercalcemia(greater than 14mg/dl), made increase of the parathyroid hormone level to greater than twice normal, and significant metabolic complications. In parathyroid cancer, systemic calcinosis is an extremely rare manifestation. The most common metastatic calcification site is lung and the other involved site is stomach, liver, skin and heart. After resection of parathyroid tumor, this systemic calcinosis is self-limiting. We experienced a patient with primary hyperparathyroidsm, presented with metastatic calcification in the lung and stomach disappeared by successful parathyroidectomy.

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  • A Case of Parathyroid Carcinoma in a Patient with Stage 3 Chronic Kidney Disease
    Youn Hee Cho, Moo Yong Park, Soo Jeong Choi, Jin Kuk Kim, Seung Duk Hwang, Jung Mi Park, Jeong Ja Kwak
    Korean Journal of Medicine.2012; 83(6): 796.     CrossRef
Acute megakaryoblastic leukemia.
Young Jin Kim, Tae Nyun Kim, Myung Soo Hyun, Bong Sup Shim, Hyun Woo Lee, Jung Suk Kim
Yeungnam Univ J Med. 1991;8(2):209-216.   Published online December 31, 1991
DOI: https://doi.org/10.12701/yujm.1991.8.2.209
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AbstractAbstract PDF
Acute megakaryoblastic leukemia is a rare and rapidly fatal disease characterized by proliferation of megakaryocyte series and atypical megakaryocytes in the bone marrow. Acute megakaryoblastic leukemia is suspicious when 1) megakaryocyte in peripheral blood, mixture of large and small mononuclear megakaryoblast in the bone marrow 2) cytoplasmic budding in blast 3) myelofibrosis (dense medullary overgrowth of reticulin fibers) 4) PAS (+), ANAE (+), SBB (−), peroxidase (−) and which is confirmed by platelet peroxidase oxidation on electron microscope or monoclonal antibody. A case of acute megakaryoblastic leukemia was studied morphologically and monoclonal antibody.

JYMS : Journal of Yeungnam Medical Science