Case Report

Korean J Hematol 2009; 44(4):

Published online December 30, 2009

https://doi.org/10.5045/kjh.2009.44.4.320

© The Korean Society of Hematology

일반적인 기본 아밀로이드 Lymphadenopathy

박진현, 권지현, 김지원, 조현진, 김기환, 정두현, 김인호, 윤성수, 박선양, 김병국

서울대학교 의과대학 내과, 병리학과, 암연구소

Generalized Primary Amyloid Lymphadenopathy

Jin Hyun Park, Ji Hyun Kwon, Ji Won Kim, Hyeon Jin Cho, Ki Hwan Kim, Doo Hyun Chung, In ho Kim, Sung Soo Yoon, Seon yang Park, Byoung Kook Kim

Cancer Research Institute,Department of Internal Medicine, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, Department of Pathology, Seoul National University College of Medicine, Seoul, Korea

Abstract

Systemic amyloidosis is a disease that displays deposition of insoluble polymeric protein fibrils in tissues and organs. We report here on a case of a 64-year-old woman who initially presented with multiple enlarged lymph nodes. Computed tomography showed multiple enlarged lymph nodes in the mediastinal, lower cervical, supraclavicular, axillary and abdominal areas. Excision biopsy of the cervical lymph nodes and the subsequent histopathology showed amorphous eosinophilic material deposits, and these revealed apple-green birefringence on a polarizing microscopic examination on the Congo-red stained slide. The patient was diagnosed with amyloidosis and she received chemotherapy consisting of melphalan and dexamethasone. During chemotherapy, she was diagnosed with breast cancer. After modified unilateral radical mastectomy, the dexamethasone was restarted and this therapy resulted in stable disease. (Korean J Hematol 2009;44:320-324.)

Keywords Systemic amyloidosis, Multiple lymph node enlargement, Chemotherapy

Article

Case Report

Korean J Hematol 2009; 44(4): 320-324

Published online December 30, 2009 https://doi.org/10.5045/kjh.2009.44.4.320

Copyright © The Korean Society of Hematology.

일반적인 기본 아밀로이드 Lymphadenopathy

박진현, 권지현, 김지원, 조현진, 김기환, 정두현, 김인호, 윤성수, 박선양, 김병국

서울대학교 의과대학 내과, 병리학과, 암연구소

Generalized Primary Amyloid Lymphadenopathy

Jin Hyun Park, Ji Hyun Kwon, Ji Won Kim, Hyeon Jin Cho, Ki Hwan Kim, Doo Hyun Chung, In ho Kim, Sung Soo Yoon, Seon yang Park, Byoung Kook Kim

Cancer Research Institute,Department of Internal Medicine, Seoul National University College of Medicine, Clinical Research Institute, Seoul National University Hospital, Department of Pathology, Seoul National University College of Medicine, Seoul, Korea

Abstract

Systemic amyloidosis is a disease that displays deposition of insoluble polymeric protein fibrils in tissues and organs. We report here on a case of a 64-year-old woman who initially presented with multiple enlarged lymph nodes. Computed tomography showed multiple enlarged lymph nodes in the mediastinal, lower cervical, supraclavicular, axillary and abdominal areas. Excision biopsy of the cervical lymph nodes and the subsequent histopathology showed amorphous eosinophilic material deposits, and these revealed apple-green birefringence on a polarizing microscopic examination on the Congo-red stained slide. The patient was diagnosed with amyloidosis and she received chemotherapy consisting of melphalan and dexamethasone. During chemotherapy, she was diagnosed with breast cancer. After modified unilateral radical mastectomy, the dexamethasone was restarted and this therapy resulted in stable disease. (Korean J Hematol 2009;44:320-324.)

Keywords: Systemic amyloidosis, Multiple lymph node enlargement, Chemotherapy

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