Sjoegren 's Syndrome Complicated with Autoimmune Hepatitis and Antiphospholipid Antibody Syndrome.

Katayama, Yoshio; Kohriyama, Kenji; Kirizuka, Keiji; Nishizaki, Hiroshi; Fujii, Hiroshi; Tanji, Yoshiaki

doi:10.2169/internalmedicine.39.73

Cited by 19 publications

(11 citation statements)

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“…Although antiphospholipid syndrome also accompanies thrombocytopenia, this patient was negative for anti-phospholipid Abs and exhibited no signs of vascular thrombosis or any other stigmata of this syndrome (15). Association ofAIH and the presence of anti-phospholipid Abs has recently been described (16,17). However, no mention has hitherto been made of antiphospholipid Ab titers in most previous reports concerning AIH patients complicated by thrombocytopenia.…”

Section: Discussionmentioning

confidence: 73%

Autoimmune Hepatitis Concomitant with Hypergammaglobulinemic Purpura, Immune Thrombocytopenia, and Sjoegren's Syndrome.

Wada¹,

Kamimoto

Park

et al. 2001

Intern. Med.

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Sjogren's syndrome occurs as an occasional complication of autoimmune hepatitis, and purpura or thrombocytopenia develops in some patients with this syndrome. This report describes a 62-year-old womanwith a 6-year history of autoimmune hepatitis who concurrently had hypergammaglobulinemic purpura, immune thrombocytopenia and Sjogren's syndrome. Treatment with prednisolone resulted in marked improvement of biochemical, hematological and dermatological abnormalities. This case emphasizes the manifestation of purpura or thrombocytopenia as an associated disorder during the course of autoimmunehepatitis concomitant with Sjogren's syndrome. (Internal Medicine 40: 308-311, 2001)

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Section: Discussionmentioning

confidence: 73%

Autoimmune Hepatitis Concomitant with Hypergammaglobulinemic Purpura, Immune Thrombocytopenia, and Sjoegren's Syndrome.

Wada¹,

Kamimoto

Park

et al. 2001

Intern. Med.

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“…Katayama et al described a case of AIH combined with Sjögren's and antiphospholipid syndromes (20). This 56-year-old Japanese female simultaneously developed thrombocytopenia, sicca symptoms, and an elevation of transaminase.…”

Section: Discussionmentioning

confidence: 96%

Systemic Autoimmune Disorders Associated with Celiac Disease

et al. 2005

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“…Antiphospholipid antibodies have been detected in 3-14% of AIH patients. 7 Katayama et al 8 with prednisolone. The patient developed lung infarction, and subsequent evaluation revealed the presence of IgM anticardiolipin antibody.…”

Section: Sirmentioning

confidence: 99%

Anti-liver and antiendomysial autoantibodies in primary antiphospholipid (Hughes’) syndrome

Rodrigues

Caleiro

Carvalho

2010

Lupus

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Anti-liver and antiendomysial autoantibodies in primary antiphospholipid (Hughes') syndrome Sir,Autoimmune hepatitis (AIH) is a chronic hepatitis of unknown etiology and it is also characterized by the presence of liver-associated autoantibodies and hypergammaglobulinemia. 1 AIH is one of the major autoimmune liver diseases (ALDs), and 20-40% of cases are associated with other autoimmune disorders. 1 The most common connective tissue disorders related to AIH is systemic lupus erythematosus. 1 However, the co-occurrence of antiphospholipid syndrome (APS) with AIH is quite rare, and only a few cases of ALD and antiphospholipid syndrome (APS) have been described.The aim of this study was to evaluate the prevalence and clinical significance of circulating anti-liver and antiendomysial autoantibodies in a cohort of patients with primary antiphospholipid syndrome (PAPS).All study participants met the 1997 revised Sapporo criteria for the diagnosis of APS. 2 This research is characterized as a descriptive crosssectional study that was conducted in the

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Sjoegren 's Syndrome Complicated with Autoimmune Hepatitis and Antiphospholipid Antibody Syndrome.

Cited by 19 publications

References 11 publications

Autoimmune Hepatitis Concomitant with Hypergammaglobulinemic Purpura, Immune Thrombocytopenia, and Sjoegren's Syndrome.

Autoimmune Hepatitis Concomitant with Hypergammaglobulinemic Purpura, Immune Thrombocytopenia, and Sjoegren's Syndrome.

Systemic Autoimmune Disorders Associated with Celiac Disease

Anti-liver and antiendomysial autoantibodies in primary antiphospholipid (Hughes’) syndrome

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