Autoimmune hepatitis

Chronic autoimmune hepatitis (AIH) is a rare progressive inflammatory disorder of unknown cause primarily affecting women and associated with circulating autoantibodies, elevated transaminase levels, and increased levels of immunoglobulin.

Pancytopenia

An abnormal reduction in numbers of all blood cell types (red blood cells, white blood cells, and platelets).


Total: 4

                       


(per page)
PMID (PMCID)
29671215
 FEMALE
A patient presenting with isolated hematuria and renal dysfunction as rare manifestation of cryoglobulinemic glomerulonephritis in the course of autoimmune diseases including Sjogren's syndrome.
Yamanaka M, Fujigaki Y, Kono H, Nagura M, Arai S, Tamura Y, Ota T, Shibata S, Kondo F, Yamaguchi Y, Uchida S.
CEN Case Rep. 2018;7(2):211-216.
We describe a case of 72-year-old woman with Hashimoto disease, autoimmune hepatitis, Sjogren's syndrome, and immune-related pancytopenia complicated by cryoglobulinemic glomerulonephritis.
21844579
 MIXED_SAMPLE Middle Aged
The utility of fluorescence in situ hybridization (FISH) analysis in diagnosing graft versus host disease following orthotopic liver transplant.
Post GR, Black JS, Cortes GY, Pollack RB, Wolff DJ, Lazarchick J.
Ann Clin Lab Sci. 2011;41(2):188-92.
We present the case of a 61 year old female who developed skin rash and pancytopenia following sex-mismatched second liver transplant for autoimmune hepatitis.
10795696
 FEMALE Middle Aged
Abnormal pulmonary accumulation of indium-111 chloride in pneumocystis carinii pneumonia as detected by bone marrow scintigraphy.
Matsuoka S, Uchiyama K, Kuniyasu Y, Niio Y, Shima H, Doai K, Oishi S, Nojiri Y, Ogata H.
Clin Nucl Med. 2000;25(5):361-3.
In-111 chloride bone marrow scintigraphy was performed to evaluate the bone marrow activity associated with pancytopenia in a 56-year-old woman with autoimmune hepatitis.
777034
 FEMALE Child
Weber-Christian panniculitis and auto-immune disease: a case report.
Allen-Mersh TG.
J Clin Pathol. 1976;29(2):144-9.
A case is described of Weber-Christian panniculitis accompanied by a gammaglobulin disturbance which preceded by five years the diagnosis of an autoimmune hepatitis and pancytopenia.