J Korean Med Sci.  2004 Feb;19(1):137-141. 10.3346/jkms.2004.19.1.137.

Adult-onset Still's Disease with Disseminated Intravascular Coagulation and Multiple Organ Dysfunctions Dramatically Treated with Cyclosporine A

Affiliations
  • 1Division of Rheumatology, The Hospital for Rheumatic Diseases, Hanyang University Medical Center, Seoul, Korea. thkim@hanyang.ac.kr

Abstract

Severe systemic manifestations of adult onset Still's disease (AOSD) are often fatal and occasionally related to hemophagocytic syndrome (HS). We describe the case of a 49-yr-old woman with AOSD presenting with non-remitting high fever, confusion, jaundice, hepatosplenomegaly, serositis, azotemia, pancytopenia, coagulopathy with disseminated intravascular coagulation (DIC), hyperferritinemia, acute acalculous cholecystitis and ileocolitis noted in computed tomographic images. The patient had a history of herpes zoster developed prior to the admission, but there is no history of diarrhea or abdominal pain. Although bone marrow examination was not performed due to hemorrhagic diathesis, we suspected AOSD-associated HS on the basis of clinical course without detectable infectious agents in cultures or serologic studies. Intravenous immunoglobulin, pulse methylprednisolone, oral cyclosporine A (CsA) and ceftriaxone brought about transient improvement of fever and confusion, but the disease progressed. After increasing CsA dose, all previously mentioned abnormalities disappeared rapidly. Accordingly, we believe that DIC and multiple organ dysfunctions might have been the complications of HS but not that of sepsis, and that CsA can be used as a first-line therapy in case of life-threatening situations.

Keyword

Still's Disease, Adult-onset; Hemophagocytic Syndrome; Cyclosporins

MeSH Terms

Colon/radiography
Cyclosporine/*therapeutic use
Female
Human
Immunosuppressive Agents/*therapeutic use
Middle Aged
*Multiple Organ Failure
Still's Disease, Adult-Onset/*diagnosis/*pathology
Time Factors
Tomography, X-Ray Computed

Figure

  • Fig. 1 Computed tomographic findings of abdomen appear acute acalculous cholecystitis and ileocolitis. (A) A thickened wall of gall bladder with pericholecytic fluid collection, (B) An unenhanced wall thickenings of cecum and terminal ileum.

  • Fig. 2 Clinical course and treatment of this patient. FFP, fresh frozen plasma; PC, platelet concentrate; PRC, packed red cell; PSL, prednisolone; IVIG, intravenous immunoglobulin; ND, not done.


Cited by  2 articles

Two Cases of Adult Onset Still's Disease with Concomitant Hemophagocytic Syndrome
Hyun-Sook Kim, Keun-Woo Park, Soo-Kyoung Kim, Ji-Young Kim, Sung Hoon Park, Jin-Hyang Shin, Sang-Gyung Kim, Jung-Yoon Choe
J Korean Rheum Assoc. 2007;14(2):160-165.    doi: 10.4078/jkra.2007.14.2.160.

Bone Marrow Findings, and TNF-α, IL-18 Expression in Bone Marrow of Adult Onset Still's Disease Patients
Kyong Hee Jung, Hye Yong Kim, Chang Nam Son, Joo Hyung Kim, Won Jun Kim, Kyeong A Lee, Ho Hyun Park, Woong Soo Lee, Dae Hyun Yoo
J Korean Rheum Assoc. 2009;16(2):87-94.    doi: 10.4078/jkra.2009.16.2.87.


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