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A Case of Neurofibromatosis with Multiple Neurofibromas on Mesentery

Hwang PG, Park SY, Whang TG, Lee SY

  • KMID: 2335212
  • J Korean Pediatr Soc.
  • 1997 Feb;40(2):270-273.
Neurofibromatosis originally described by von-Recklinhausen in 1882, is often depicted as a chronic progressive hereditary disease characterized by pigmentation of the skin, cutaneus lesions, and numerous tumors developing in association...
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Endometrial Mucinous Adenocarcinoma with Extensive Squamous Differentiation: A Case Report

Lee HC, Hwang PG, Cho SY, Park YS, Park IA

  • KMID: 1979375
  • Korean J Pathol.
  • 2003 Dec;37(6):438-441.
Endometrial mucinous adenocarcinoma occurs in 1-9% of endometrial adenocarcinomas and adenocarcinoma with squamous differentiation in approximately 25%. We report a rare case of mucinous adenocarcinoma with squamous differentiation in a...
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Hydrops Fetalis Due to Parvovirus B19 Infection: Report of Two Autopsy Cases

Lee HC, Lee HE, Hwang PG, Chi JG, Park SH

  • KMID: 2277674
  • Korean J Pathol.
  • 2006 Jun;40(3):245-249.
Hydrops fetalis (HF) is a disease characterized by generalized subcutaneous edema and cavity effusion in the fetal stage. We report here on two autopsy cases of HF that were caused...
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Death Associate with Sweet's Syndrome

Li Z, Hwang PG, Lee YS, Lee JB, Lee SD

  • KMID: 1849287
  • Korean J Leg Med.
  • 2003 Oct;27(2):82-86.
Sweet's syndrome was originally described as an "acute febrile neutrophilic dermatosis". Sweet's syndrome presents in three clinically settings: (1) classical or idiopathic Sweet's syndrome, (2) malignancyassociated or paraneoplastic Sweet's syndrome,...
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Dedifferentiated Chondrosarcoma with Giant Cell-rich Sarcomatous Component Resembling Giant Cell Tumor: A Case Report

Hwang PG, Won JK, Kim MA, Kim HS, Lee SH, Kim CJ

  • KMID: 2073849
  • Korean J Pathol.
  • 2004 Oct;38(5):345-349.
Dedifferentiated chondrosarcoma is an uncommon bone tumor, defined as a tumor in which two components -a low-grade chondrosarcoma and a high-grade non-cartilaginous sarcoma-coexist with abrupt interface. We report a rare...
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