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"Jang Won Park"

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"Jang Won Park"

Case Reports
[English]
Diffuse Large B-Cell Lymphoma Transformed from a Rectal Mucosa-Associated Lymphoid Tissue Lymphoma
Sae Han Kang, Jang Won Park, Byung Wook Jung, Jun Gyu Song, Hyun Sik Oh, Kwonoh Park
Ewha Med J 2016;39(2):51-55.   Published online April 29, 2016
DOI: https://doi.org/10.12771/emj.2016.39.2.51

Primary rectal lymphoma is a rare disease among the gastrointestinal (GI) lymphoma. In particular, diffuse large B-cell lymphoma (DLBCL) transformed from mucosa-associated lymphoid tissue (MALT) lymphoma is often the primary type of GI lymphoma, mostly in stomach or duodenum, but has never been reported in rectum. Here we report an unusual case in which a 75-year-old male patient diagnosed with DLBCL transformed from MALT lymphoma in the rectum. The patient was diagnosed as rectal DLBCL transformed from MALT lymphoma as Lugano stage II2 and was treated with chemotherapy (R-CHOP) with CD-20 monoclonal antibody (rituxaimb). Complete remission of multiple lymphadenopathy and mass forming ulcer of the rectum was achieved after 6 cycles of R-CHOP. He has been free from disease for 12 months.

Citations

Citations to this article as recorded by  
  • Clinical Characteristics and Long-Term Prognosis of Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma According to the Endoscopic Classification and Treatment Modality: A Multicenter Study
    Seung Min Hong, Dong Hoon Baek, Geun Am Song, Hong Sub Lee, Seung Bum Lee, Ra Ri Cha, Tae-Oh Kim, Jae Hyun Kim, Jong Hoon Lee
    Cancers.2025; 17(5): 750.     CrossRef
  • 107 View
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  • 1 Crossref
[English]
Pulmonary Tumor Thrombotic Microangiopathy Associated with Advanced Gastric Cancer Successfully Treated with Chemotherapy
Seung-Hyun Yoo, Kwonoh Park, Ji Yeon Hong, Ji Yeon Kim, Jang Won Park, Yong Won Park, Kyung-Hun Lee, Kyung-So Jeon
Ewha Med J 2014;37(2):146-151.   Published online September 30, 2014
DOI: https://doi.org/10.12771/emj.2014.37.2.146

Pulmonary tumor thrombotic microangiopathy (PTTM) is an uncommon and fatal malignancy-related pulmonary complication characterized by fibrocellular intimal proliferation of small pulmonary arteries and arterioles. It causes marked pulmonary hypertension, right-side heart failure, and sudden death. Diagnosis of PTTM is extremely difficult while the patient is alive. Here, we report a 44-year-old woman who presented with complaining of progressing dyspnea and pulmonary hypertension but with no history of cancer. She was diagnosed with PTTM caused by advanced gastric cancer ante mortem and was treated effectively with chemotherapy.

Citations

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  • Pulmonary Tumor Thrombotic Microangiopathy Associated With Gastric Cancer: Clinical Characteristics and Outcomes
    Tae-Se Kim, Soomin Ahn, Sung-A Chang, Sung Hee Lim, Byung-Hoon Min, Yang Won Min, Hyuk Lee, Poong-Lyul Rhee, Jae J. Kim, Jun Haeng Lee
    Journal of Gastric Cancer.2025;[Epub]     CrossRef
  • Sudden Development of Fatal Pulmonary due to Suspected Pulmonary Tumoral Thrombotic Microangiopathy among Patients with Cancer: Case Series of Clinical and CT Features in 10 Patients
    Bo Kyung Kim, Yookyung Kim, Kyung Eun Lee
    Journal of the Korean Society of Radiology.2024; 85(6): 1169.     CrossRef
  • 137 View
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  • 2 Crossref
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