Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

149 results
Display

Multiple Ecthyma Gangrenosum in a Hemophagocytic Lymphohistiocytosis Patient

Park BM, Yun SJ, Han DK, Kook H, Lee JB, Lee SC, Won YH, Kim SJ

  • KMID: 2247248
  • Korean J Dermatol.
  • 2013 Mar;51(3):223-224.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two Cases of Hemophagocytic Lymphohistiocytosis Following Kikuchi's Disease

Kim JW

  • KMID: 2302218
  • Korean J Dermatol.
  • 2007 May;45(5):471-476.
Kikuchi's disease is a benign, self-limiting, acute, necrotizing lymphadenitis predominantly occurring in young women in Asia. Hemophagocytic lymphohistiocytosis (HLH), previously known as hemophagocytic syndrome, describes the pathologic phenomenon of activated...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hemophagocytic lymphohistiocytosis secondary to histoplasmosis

Karthik Bommanan BK, Naseem S, Varma N

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hemophagocytic Lymphohistiocytosis

Park SY, Lee JM

Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal disease caused by dysregulated immune responses and overwhelming inflammation to infectious or other triggers of the immune system. HLH may be inherited (primary)...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of Wegener's granulomatosis mimicking recurrent hemophagocytic lymphohistiocytosis

Jung SM, Jung YH, Noh HJ, Woo IS, Han CW

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hemophagocytic Lymphohistiocytosis Manifesting as a Purpuric Patch

Lyu SM, Byun JY, Choi YW, Choi HY

  • KMID: 1732328
  • Korean J Dermatol.
  • 2014 Jun;52(6):421-424.
Hemophagocytic lymphohistiocytosis (HLH) is a fatal, systemic inflammatory syndrome that characteristically presents hemophagocytic histiocytes infiltrating into various organs. Common features of HLH are abrupt onset of high fever, malaise, lymphadenopathy,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Secondary Precursor B-cell Acute Lymphoblastic Leukemia Occurring after Treatment of Hemophagocytic Lymphohistiocytosis

Yang SI, Jeon IS

  • KMID: 1448325
  • Clin Pediatr Hematol Oncol.
  • 2011 Oct;18(2):140-143.
Hemophagocytic lymphohistiocytosis (HLH), although uncommon, is illustrated as a dramatic clinical presentation of multi-systemic inflammation due to the impaired activity of cytotoxic T-cell and NK cell. Etoposide, an important component...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
CNS Involvement in Hemophagocytic Lymphohistiocytosis: CT and MR Findings

Chung TW

Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder that is characterized by proliferation of benign histiocytes, and this commonly involves the liver, spleen, lymph nodes, bone marrow and central nervous system...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Parvovirus B19 infection-associated hemophagocytic lymphohistiocytosis

Shim H, Kim HJ, Lee YJ, Park MR

  • KMID: 1962209
  • Korean J Med.
  • 2007 Apr;72(4):433-436.
Hemophagocytic lymphohistiocytosis is an unusual syndrome that's characterized by fever, hepatosplenomegaly, cytopenias, hypertriglyceridemia, hypofibrinogenemia and pathologic finding of hemophagocytosis in the bone marrow and other tissues. A previously healthy 16-year-old...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two cases of bacteria associated hemophagocytic syndrome in typhoidfever

Shin BM

  • KMID: 1685060
  • Korean J Clin Pathol.
  • 1993 Mar;13(1):43-48.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two cases of bacteria associated hemophagocytic syndrome in typhoidfever

Shin BM

  • KMID: 1684971
  • Korean J Clin Pathol.
  • 1992 Mar;12(1):43-48.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Hemophagocytosis in the pleural fluid of a patient with hemophagocytic lymphohistiocytosis

Chang EJ, Kim TE, Jeon IS

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two Cases of Severe Fever with Thrombocytopenia Syndrome Manifested with Hemophagocytic Lymphohistiocytosis Successfully Treated with Steroids

Kim YJ, Bae SH, Jung HJ, Lee SA, Kim MJ, Chang HH, Kim SW, Kim SJ, Lee JM

Severe fever with thrombocytopenia syndrome (SFTS) is an emerging and potentially life-threatening tick-borne virus disease in Korea. It can be presented with hemophagocytic lymphohistiocytosis (HLH) as severe complicated cases. Here,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Preceding Annular Skin Lesions in a Patient with Hemophagocytic Lymphohistiocytosis

Jun HJ, Kim HO, Lee JY, Park YM

The cutaneous manifestations of hemophagocytic lymphohistiocytosis (HLH) are variable and nonspecific. A 42-year-old man presented with multiple annular, erythematous patches on the trunk for 3 months. Two months later, he...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Death Due to Hemophagocytic Lymphohistiocytosis Accompanied by Scrub Typhus

Kim HW, Choi BS, Kim JH, Shin YM, Lee SJ, Kim SR, Jun JB

Hemophagocytic lymphohistiocytosis (HLH) is a rare disease with a high mortality rate. It is associated with a variety of bacterial, viral, fungal, and parasitic infections. In the literature, there are...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Hemophagocytic Syndrome Induced by Adenovirus Infection after Splenectomy

Park SH, Lee KS

  • KMID: 2168958
  • Clin Pediatr Hematol Oncol.
  • 2009 Apr;16(1):49-53.
Hemophagocytic lymphohistiocytosis (HLH) is a rare but sometimes fatal disease. Its main features are prolonged fever, hepatosplenomegaly, cytopenias, and hemophagocytosis in the bone marrow, lymph nodes and other tissues. Hemophagocytic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Hemophagocytic Lymphohistiocytosis in a Child with Systemic Lupus Erythematosus

Hwang JY, No SM, Lee J, Jang PS, Kim YH, Kim JT, Lee JS

  • KMID: 2206976
  • J Korean Pediatr Soc.
  • 2003 Oct;46(10):1029-1031.
Hemophagocytic lymphohistiocytosis is a reactive disorder characterized by a generalized non-malignant histiocytic proliferation with prominent hemophagocytosis by stimulated histiocytes in the bone marrow and reticuloendothelial systems resulting in pancytopenia and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Chronic Graft-Versus-Host Disease Mimicking Psoriasis in a Patient with Hemophagocytic Lymphohistiocytosis

Jang S, Kim IS, Youn SW

Graft-versus-host disease (GVHD) is a common complication of bone marrow transplantation (BMT) that can be classified as acute or chronic. Chronic GVHD, which usually occurs more than 3 months after...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of hepatitis B virus-associated hemophagocytic syndrome

Choi YM, Kim JW, Lim KS

  • KMID: 1697918
  • Korean J Intern Med.
  • 1991 Jun;40(6):838-843.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acute Human Immunodeficiency Virus Syndrome Presenting with Hemophagocytic Lymphohistiocytosis

Park KH, Yu HS, Jung SI, Shin DH, Shin JH

Hemophagocytic lymphohistiocytosis (HLH) has been described in patients with advanced stages of human immunodeficiency virus (HIV) infection, but rarely occurs during the seroconversion stage of acute HIV infection. We report...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr