- A Case of Rheumatoid Pneumoconiosis Presenting with Pleuritis and Pericarditis
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Park MS, Kang DG, Jung EJ, Oh KJ, Sim JS, Kim EJ, Kim C
- KMID: 1833856
- Korean J Med.
- 2013 Mar;84(3):428-432.
- doi: 10.3904/kjm.2013.84.3.428
Caplan's syndrome is characterized by multiple small distinct nodules with progressive massive fibrosis and rheumatic arthritis in pneumoconiosis. Although pleural effusions occur infrequently as an extra-articular manifestation, pleuritis can develop... -
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- A case of systemic lupus erythematosus presented with refractory serositis and nephritis during pregnancy
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Park HR, Song JS, Shin JI, Park BH, Park W
- KMID: 1927332
- Korean J Med.
- 2004 Nov;67(Suppl 3):S896-S901.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibodies and immune complex depositions, has been known that it could be aggravated during pregnancy. We report a case who... -
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- Systemic Lupus Erythematosus: Abdominal Radiologic Findings
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Oh JC, Cho OK, Lee YJ, Bae JI, Kim YS, Rhim HC, Ko BH
- KMID: 2200943
- J Korean Radiol Soc.
- 1999 Jun;40(6):1173-1179.
- doi: 10.3348/jkrs.1999.40.6.1173
Systemic lupus erythematosus(SLE) is a systemic disease of unknown etiology. Its main pathology is vasculitis and serositis, due to deposition of the immune complex or antibodies. Most findings are nonspecific... -
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- A Case of Erythema Nodosum and Serositis Associated with Myelodysplastic Syndrome
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Choi JH, Ahn MJ, Park YW, Oh HS, Lee YY, Kim IS
- KMID: 1718043
- Korean J Intern Med.
- 2005 Jun;20(2):177-179.
- doi: 10.3904/kjim.2005.20.2.177
Myelodysplastic syndrome (MDS) is a heterogenous group of stem cell disorders usually characterized by progressive refractory cytopenias, which could progress to acute myeloid leukemia. MDS may be associated with a... -
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- Adult Onset Still's Disease
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Lee DH, Park JW, Hyun JW, Kim DH, Suh YS
- KMID: 2294530
- J Korean Acad Fam Med.
- 2007 Mar;28(3):210-213.
Adult onset Still's disease (AOSD) is an uncommon acute systemic inflammatory disease of unknown origin. The clinical features include high spiking fever, arthralgia or arthritis, transient maculopapular rash, lymphadenopathy, hepatosplenomegaly,... -
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- A Case of Adult-Onset Still's Disease Presented with Urticaria
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Hong KK, Lew BL, Yang YI, Kim NI
- KMID: 2302356
- Korean J Dermatol.
- 2006 Jan;44(1):63-66.
Adult-onset Still's diseas e(AOSD) is a rare, systemic inflammatory disease of unknown etiology, characterized by spiking fever, skin rash, arthralgia or arthritis, lymphadenopathy, hepatosplenomegaly, sore throat and serositis. The typical... -
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- A Case of Cytophagic Histiocytic Panniculitis Involving the Extrapleural Fat
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Seo JK, Choi JH, Lee SM, Lee SK
- KMID: 2302244
- Korean J Dermatol.
- 2007 Feb;45(2):180-184.
Cytophagic histiocytic panniculitis gap (CHP) was described in 1980 as a chronic histiocytic disease of the subcutaneous tissue and associated with systemic manifestations such as fever, serositis, and hepatosplenomegaly. The... -
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- Systemic Lupus Erythematosus with Initial Presentation of Ascites
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Chu JM, Kang SH, Song JH, Han KH, Shin SY, Yang TY, Choi JJ, Hong SP
- KMID: 2171295
- Ewha Med J.
- 2014 Sep;37(2):121-125.
- doi: 10.12771/emj.2014.37.2.121
Systemic lupus erythematosus (SLE) is a chronic inflammatory disease of unknown etiology and is characterized by presence of variable pathogenic auto-antibodies and multiple organ involvement. Serositis is common in SLE,... -
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- A Case of recurrent adult onset still's disease with interstitial pneumonitis
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Ryoo ES, Moon SH, Bae SB, Kim SG, Lee GG, Hong GY, Lee TY, Kim JS, Kim HT
- KMID: 2251371
- Korean J Med.
- 1999 Aug;57(2):220-224.
Adult onset Still's disease(AOSD) is characterized by a high spiking fever, a transient rash, and arthritis. The clinical features include lymphadenopathy, hepatospleno-megaly, serositis, and sore throat. Leukocytosis is generally marked,... -
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- Adult Onset Still's Disesae: A Case Report
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Kim BJ, Kim SY, Kim GM
- KMID: 2301955
- Korean J Dermatol.
- 2009 Oct;47(10):1203-1205.
Adult-onset Still's disease (AOSD) is a systemic inflammatory disease of an unknown etiology, and AOSD is characterized by high fever, skin rash, arthritis, lymphadenopathy, hepatomegaly, sore throat and serositis. The... -
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- Autoinflammatory Diseases
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Lee SH
- KMID: 2222945
- J Rheum Dis.
- 2014 Oct;21(5):228-235.
- doi: 10.4078/jrd.2014.21.5.228
Autoinflammatory diseases (AIDs) refer to a broad range of genetically mediated conditions characterized by recurrent attacks of systemic inflammation with typical manifestations of fever, rash, serositis, lymphadenopathy, and musculoskeletal symptoms.... -
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- Familial Mediterranean fever presenting as fever of unknown origin in Korea
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Lee JH, Kim JH, Shim JO, Lee KC, Lee JW, Lee JH, Chae JJ
- KMID: 2362255
- Korean J Pediatr.
- 2016 Nov;59(Suppl 1):S53-S56.
- doi: 10.3345/kjp.2016.59.11.S53
Familial Mediterranean fever (FMF) is the most common Mendelian autoinflammatory disease, characterized by uncontrolled activation of the innate immune system that manifests as recurrent brief fever and polyserositis (e.g., peritonitis,... -
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- A Case of Intravascular Large B-cell Lymphoma Mimicking Systemic Lupus Erythematosus
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Park CK, Lee JC, Kang SW, Shim SC, Yun HJ, Kim JM, Yoo IS
- KMID: 2268938
- Korean J Med.
- 2015 Dec;89(6):746-751.
- doi: 10.3904/kjm.2015.89.6.746
Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin's lymphoma (NHL) and that progresses rapidly and is usually fatal. Because it usually presents with nonspecific symptoms, such as... -
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- Familial Mediterranean Fever With Complete Symptomatic Remission During Pregnancy
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Kim KT, Jang HJ, Lee JE, Kim MK, Yoo JJ, Lee GY, Kae SH, Lee J
- KMID: 2174490
- Intest Res.
- 2015 Jul;13(3):287-290.
- doi: 10.5217/ir.2015.13.3.287
Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically restricted and commonly found among populations surrounding the Mediterranean Sea. FMF is the most prevalent autoinflammatory disease; is characterized... -
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- The technique and the safety of laparoscopic incidental appendectomy using single loop during gynecologic laparoscopic surgery
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Kim JJ, Kim DH, Lee SH, Park MY, Lee MK, Kim JY, Chung RJ
- KMID: 2273181
- Korean J Obstet Gynecol.
- 2007 Sep;50(9):1254-1259.
OBJECTIVE: To introduce the technique of laparoscopic incidental appendectomy using single loop during gynecologic laparoscopic surgery and to demonstrate the safety of it. METHODS: This was a retrospective case-controlled study of... -
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- Clinical Manifestations On Systemic Lupus Erythematosus
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Chun JH, Shin KC, Park CW, Doh GS, Lee CK, Hyun MS, Lee HW, Kim NS, Kim HC
- KMID: 2334732
- J Korean Rheum Assoc.
- 1994 Jul;1(2):159-168.
OBJECTIVE: Systemic lupus erythematceus(SLE) is an autoimmune disease and manifests with a variety of clinical and immunologic features in the multisystem SLE occurs worldwide in all ethnic groups but the... -
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- A Case of Adult-onset Still's Disease associated with Congestive Heart Failure
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Park BH, Min JY, Yeo CD, Oh SS, Hur KH, Hur SE, Kim JS, Kim WC, Kim WU
- KMID: 2334819
- J Korean Rheum Assoc.
- 2005 Sep;12(3):235-239.
Adult onset Still's disease (AOSD) is a multi-systemic inflammatory disorder characterized by several distinguished manifestations including high spiking fever, evanescent salmon-colored skin rash, arthralgia/arthritis, hepato-splenomegaly, lymphadenopathy, sore throat, serositis, and... -
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- An Unusual Case of Severe Neonatal Lupus Mimicking Neonatal Sepsis and Literature Review
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Park HM, Jun HG, Park JH, Choi SW, Oh KW, Oh JS
- KMID: 2297529
- J Rheum Dis.
- 2014 Jun;21(3):156-161.
- doi: 10.4078/jrd.2014.21.3.156
Neonatal lupus is an uncommon autoimmune disease that results from transplacental passage of the maternal anti-SSA/Ro and/or anti-SSB/La antibodies. Pancytopenia or severe jaundice is a rare manifestation of neonatal lupus,... -
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- Pathogenesis and clinical manifestations of juvenile rheumatoid arthritis
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Hahn YS, Kim JG
- KMID: 2280904
- Korean J Pediatr.
- 2010 Nov;53(11):921-930.
- doi: 10.3345/kjp.2010.53.11.921
Juvenile rheumatoid arthritis (JRA) is the most common rheumatic childhood disease; its onset is before 16 years of age and it persists for at least 6 weeks. JRA encompasses a... -
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- A Case of Successful Treatments of Venous Leg Ulcers in Secondary Antiphospholipid Syndrome
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Kim BK, Choi ST, Son MK, Lee KH, Lee SW, Chung SJ, Gil JH, Park YB, Lee SK
- KMID: 2202193
- J Korean Rheum Assoc.
- 2007 Mar;14(1):71-77.
- doi: 10.4078/jkra.2007.14.1.71
Antiphospholipid syndrome is an autoimmune disorder characterized by recurrent arterial or venous thrombosis, and pregnancy loss. A 57-year-old woman was admitted for aggravation of both leg ulcers. Venogram showed chronic... -
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