- Cutaneous Plasmacytosis with Multiple Nodular Eruptions and Polyclonal Hypergammaglobulinemia
-
Jung SY, Koh WS, Moon SE, Cho KH, Youn JI, Lee YS
- KMID: 2361457
- Ann Dermatol.
- 1994 Jul;6(2):183-187.
- doi: 10.5021/ad.1994.6.2.183
We report two patients with multiple peculiar skin eruptions and polyclonal hypergammaglobulinemia. Both patients visited our hospital for the evaluation of asymptomatic multiple nodular eruptions on almost their entire body... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Eosinophilic Fasciitis
-
Lee DH, Kim JH, Lee WB, Lee JS
- KMID: 2335168
- J Korean Pediatr Soc.
- 1996 Jan;39(1):120-125.
Eosinophilic faciitis is a recently recognized entity causing inflammation, thickening and fibrosis of the fascia, which is associated with hypergammaglobulinemia, peripheral eosinolhila. This case of 11 year-old male patient... -
- CITED
-
- Close
- SHARE
-
- Close
- One case of Autoimmune Hemolytic Anemia
-
kim SY, Park SC, Kim BG, Yoon SH, Jo JD
- KMID: 2142504
- J Korean Pediatr Soc.
- 1980 Oct;23(10):822-827.
We reviewed one case of AHA in 14 year old female child which followed a chronic course. The patient showed hypergammaglobulinemia with elevated IgM, positive direct coomb's test and positive... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Chronic Granulomatous Disease Which is Improved by Interferon- Therapy
-
Kim JC, Park SS, Yun MJ, Keum DH
- KMID: 2335259
- J Korean Pediatr Soc.
- 1997 Jul;40(7):1021-1025.
Chronic granulomatous disease is a group of rare disorders characterized by a disease of oxidative metabolism of phagocytes with deficit of antimicrobial activity. Also, it has clinical features of chronic... -
- CITED
-
- Close
- SHARE
-
- Close
- Cutaneous and Systemic Plasmacytosis Associated with Renal Amyloidosis
-
Lee TG, Jeong WS, Moon SH, Hwangbo H, Lee SK, Lee DR, Kwon TG
- KMID: 2157456
- Ann Dermatol.
- 2015 Dec;27(6):759-762.
- doi: 10.5021/ad.2015.27.6.759
Cutaneous and systemic plasmacytosis (CSP) is a rare disorder of unknown etiology characterized by cutaneous polyclonal plasma cell infiltrates associated with various extracutaneous involvement and polyclonal hypergammaglobulinemia. Here, we report... -
- CITED
-
- Close
- SHARE
-
- Close
- Eoxinophilic FAsciitis: Report of a case
-
Lee JB, Kim SC, Kim YK
- KMID: 1678086
- Korean J Dermatol.
- 1980 Aug;18(4):361-365.
Eosinophilic fasciitis is a syndrome which is characterized by scleroderma-like skin involvement, eosinophilia and hypergammaglobulinemia without significant systemic changes. The primary pathological alterations are thickening and inflammation of the deep... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Non Secretory Type Multiple Myeloma Associated with Systemic Lupus Erythematosus
-
Jeong YJ, Kim HS, Kim EJ, Kim YS, Park CY, Shin BS, Park G
- KMID: 2201904
- J Korean Rheum Assoc.
- 2010 Dec;17(4):431-436.
- doi: 10.4078/jkra.2010.17.4.431
The development of malignant tumors is a more frequent finding in lupus patients than the general population. However, the incidence of multiple myeloma associated with systemic lupus erythematosus (SLE) is... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Eosinophilic Fasciitis
-
Park MK, Jeon SJ, Suh KS, Kim ST
- KMID: 2085678
- Korean J Dermatol.
- 1989 Dec;27(6):729-733.
We report a case of eosinophilic fasciitis occurring in a 48-year-old man who showed tender, edemstous, indurated, and tight skin on the left forearm and elbow joint. Laboratory findings showed... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Hypergammaglobulinemic Purpura of Waldenstrom
-
Lim MK, Jang HS, Kwon KS, Chung TA
- KMID: 2085820
- Korean J Dermatol.
- 1995 Aug;33(4):789-793.
Hypergammaglobulinemic purpura of Waldenstrom is characterized by recurrent episodes of petechiae, hypergammaglobulinemia, an elevated erythrocyte sedimentation rate, and the presence of rheumatoid factor, and leukocytoclastic vasculitis or mild lymphocytic perivasculitis.... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Autoimmune Hepatitis
-
Park JA, Moon IH, Kim DY
- KMID: 2170945
- Ewha Med J.
- 1998 Sep;21(3):127-131.
- doi: 10.12771/emj.1998.21.3.127
Autoimmune hepatitis is a rare cause of chronic hepatitis in Korea. The cause of autoimmune hepatitis is unknown. A loss of tolerance to autologous liver tissue is regarded as the... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Cutaneous and Systemic Plasmacytosis with an Unusual Clinical Presentation
-
Lee DW, Yang JH, Won CH, Chang SE, Lee MW, Choi JH, Moon KC
- KMID: 2247894
- Korean J Dermatol.
- 2009 May;47(5):558-561.
Cutaneous and systemic plasmacytosis is a rare disorder that's characterized by a cutaneous plasma cell infiltrate accompanied by polyclonal hypergammaglobulinemia. Clinically, it appears as multiple red-brown plaques that mainly occur... -
- CITED
-
- Close
- SHARE
-
- Close
- Autoimmune Hepatitis: Recent Korean Trend
-
Lee YS
- KMID: 2183551
- J Korean Med Assoc.
- 2005 May;48(5):456-464.
- doi: 10.5124/jkma.2005.48.5.456
Autoimmune hepatitis is defined as an unresolving, predominantly periportal hepatitis of unknown etiology, usually with hypergammaglobulinemia and tissue autoantibodies, which is responsive to immunosuppressive therapy. Clinical manifestations, diagnostic criteria, differential... -
- CITED
-
- Close
- SHARE
-
- Close
- Sinus Histiocytosis with Massive Lymphadenopathy : Report of A Case with Perineal Involvement
-
Baick SE, Yang MH, Kim TC
- KMID: 1911347
- Korean J Urol.
- 1981 Aug;22(4):480-483.
The term "sinus histiocytosis with massive lyrnphadenopathy," introduced in 1969 by Rosai and Dorfman, refers to a newly recognized disease entity characterized by painless cervical lymphadenopathy, fever, leukocytosis, increased erythrocyte... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Overlap Syndromebetween Autoimmune Hepatitis and Primary Biliary Cirrhosis
-
Park SY, Jeong SA, Jeong HK, Lee HC, Lee SY, Kim DY, Moon IW, Seong SH
- KMID: 2084894
- Korean J Gastroenterol.
- 1999 Jan;33(1):148-152.
Autoimmune hepatitis is an unresolving inflammation of the liver due to unknown cause. It is characterized by hypergammaglobulinemia, and autoantibodies in serum and the presence of hepatitis that is periportal... -
- CITED
-
- Close
- SHARE
-
- Close
- Eosinophilic Fasciitis Localized on the Left Lower Extremity: A case report
-
Jeong HJ
- KMID: 2324606
- J Korean Acad Rehabil Med.
- 2007 Aug;31(4):478-481.
Eosinophilic fasciitis is a rare disorder which can markedly affect the quality of life in individual patients by disabling joint mobility. Eosinophilic fasciitis causes symmetrical pain, swelling and contracture of... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of hypocomplementemic urticarial vasculitis syndrome with cold urticaria
-
Eom JY, Yu HD, Kim NI, Haw CR
- KMID: 1693101
- Korean J Dermatol.
- 1992 Feb;30(1):87-92.
A 38-year-old man presented with a 2-year history of recurreit irticaria, abdominal pain and arthralgia of his finger joints. These symptoms were not con rolled in spite of taking medication... -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical Features of Autoimmune Hepatitis in Korea
-
Hyun JG, Paik SW, Lee JH, Koh KC, Kim JE, Choi MS, Rhee PL, Kim JJ, Rhee JC, Choi KW, Oh YL, Park CK
- KMID: 2240442
- Korean J Gastroenterol.
- 1999 May;33(5):653-661.
BACKGROUND/AIMS: Although autoimmune hepatitis (AIH) is common in western countries, only sporadic cases have been reported in Korea. The aims of the study were to analyze the clinical and histological... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Cutaneous Rosai-Dorfman Disease
-
Chung HJ, Roh MR, Lee MG, Chung KY
- KMID: 2086808
- Korean J Dermatol.
- 2004 Apr;42(4):464-468.
Rosai-Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy (SHML) is a benign, idiopathic histiocytic proliferative disorder affecting lymph nodes as well as extranodal sites. It is accompanied by fever,... -
- CITED
-
- Close
- SHARE
-
- Close
- The Castlemen's Disease in Mediastinum: A Case Report
-
Yoon HS, Jang GG, Kang JS, Kim H
- KMID: 1581866
- Korean J Thorac Cardiovasc Surg.
- 2000 Mar;33(3):265-267.
Castleman's disease is a relatively rate disorder of lymphoid tissue and poorly understood etiology. The disease may occur anywhere along the lymphatic chain, but is most commonly found as a solitary mass... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of concomitant epstein-barr virus-induced hepatitis on chronic autoimmune hepatitis
-
Jung JG, Moon DG, Yang HJ, Kwon JH, Kang JH, Jung ES, Yoon SK
- KMID: 2256198
- Korean J Med.
- 2008 Jun;74(6):658-662.
Autoimmune hepatitis (AIH), a rare cause of chronic liver disease in Korea, is a chronic, predominantly periportal hepatitis characterized by hypergammaglobulinemia, tissue autoantibodies, and responsiveness to immunosuppressive therapy. Here we... -
- CITED
-
- Close
- SHARE
-
- Close
