Immune thrombocytopenic purpura

Immune thrombocytopenic purpura (or immune thrombocytopenia; ITP) is an autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.

Hemolytic anemia

A type of anemia caused by premature destruction of red blood cells (hemolysis).


Total: 22

                       


(per page)
PMID (PMCID)
28875001
(5575730)
 OTHER
Immune Thrombocytopenic Purpura and Hemolytic Anemia Secondary to Hepatitis A.
Miri-Aliabad G, Rashidi S.
Int J Hematol Oncol Stem Cell Res. 2017;11(2):89-91.
Immune Thrombocytopenic Purpura and Hemolytic Anemia Secondary to Hepatitis A.
28875001
(5575730)
 OTHER
Immune Thrombocytopenic Purpura and Hemolytic Anemia Secondary to Hepatitis A.
Miri-Aliabad G, Rashidi S.
Int J Hematol Oncol Stem Cell Res. 2017;11(2):89-91.
In this paper, we report the case of a 3-year-old girl who developed immune thrombocytopenic purpura (ITP) and hemolytic anemia after HAV infection.
28905389
 FEMALE Middle Aged
The first reported case of concurrent trimethoprim-sulfamethoxazole-induced immune hemolytic anemia and thrombocytopenia.
Linnik YA, Tsui EW, Martin IW, Szczepiorkowski ZM, Denomme GA, Gottschall JL, Hill JM Jr, Dunbar NM.
Transfusion. 2017;57(12):2937-2941.
Drug-induced immune hemolytic anemia (DIIHA) and drug-induced immune thrombocytopenia (DIIT) are rare but dangerous complications of pharmacotherapy that may be underrecognized in hematopoietic stem cell transplant (HSCT) patients due to overlap of signs and symptoms with those of more common disease processes.
27835759
(5233712)
 MIXED_SAMPLE Adult
Zika virus epidemic in Brazil. I. Fatal disease in adults: Clinical and laboratorial aspects.
Azevedo RS, Araujo MT, Martins Filho AJ, Oliveira CS, Nunes BT, Cruz AC, Nascimento AG, Medeiros RC, Caldas CA, Araujo FC, Quaresma JA, Vasconcelos BC, Queiroz MG, da Rosa ES, Henriques DF, Silva EV, Chiang JO, Martins LC, Medeiros DB, Lima JA, Nunes MR, Cardoso JF, Silva SP, Shi PY, Tesh RB, Rodrigues SG, Vasconcelos PF.
J Clin Virol. 2016;85:56-64.
A blood sample taken on the seventh day of her illness was positive RT-PCR for ZIKV RNA and research in the serum was positive for antinuclear factor fine speckled (1/640), suggesting Evans syndrome (hemolytic anemia an autoimmune disorder with immune thrombocytopenic purpura) secondary to ZIKV infection.
26251154
 MIXED_SAMPLE Middle Aged
[Successful second cord blood transplantation (CBT) for late graft failure associated with several immune disorders after the initial CBT in a patient with acute myeloid leukemia].
Mori M, Yonezawa A, Kitagawa T, Sasaki Y, Onaka T, Imada K.
Rinsho Ketsueki. 2015;56(7):889-94.
She was diagnosed as having secondary graft failure associated with Coombs-positive immune hemolytic anemia and immune thrombocytopenia (ITP).
24942015
 MIXED_SAMPLE Infant
Congenital ADAMTS13 deficiency: a rare mimicker of immune thrombocytopenic purpura.
Quintero V, Garcia-Pose A, Barrios-Tascon A, Pacheco-Cumani M.
J Pediatr Hematol Oncol. 2014;36(8):653-5.
Mild cases of ADAMTS13 deficiency may be initially confused with immune thrombocytopenic purpura if hemolytic anemia is not severe and renal or neurological symptoms are not present.
25125734
 MALE Middle Aged
The endemic mimic: blastomycosis an illness often misdiagnosed.
Bradsher RW Jr.
Trans Am Clin Climatol Assoc. 2014;125:188-202; discussion 202-3.
In our series, cases of laryngeal carcinoma, adrenal insufficiency, thyroid nodules, granulomatous hypercalcemia, abnormal mammograms thought to represent breast carcinoma, otitis media with cranial extension, immune thrombocytopenic purpura, and hemolytic anemia of unknown cause have been misdiagnosed and blastomycosis subsequently identified as the cause.
23676145
 MALE
Aspergillosis after liver transplantation in the context of common variable immunodeficiency: case report.
Chen Y, Cameron A.
Transpl Infect Dis. 2013;15(5):540-4.
Although it mainly manifests in immunodeficiency and related infection, CVID can also be associated with autoimmune phenomena such as immune thrombocytopenic purpura, hemolytic anemia, rheumatoid arthritis, lupus, primary biliary cirrhosis, and autoimmune hepatitis (AIH).
17943645
 FEMALE Adult
A case of Evan's syndrome in pregnancy refractory to primary treatment options.
Boren T, Reyes C, Montenegro R, Raimer K.
J Matern Fetal Neonatal Med. 2007;20(11):843-5.
Evan's syndrome is a rare hematological condition defined as immune thrombocytopenic purpura and hemolytic anemia.
17506095
 MALE
Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndrome.
Gidwani P, Segal E, Shanske A, Driscoll C.
Am J Med Genet A. 2007;143A(12):1338-41.
Multiple autoimmune abnormalities are described in KS such as immune thrombocytopenic purpura (ITP), vitiligo, thyroiditis, hemolytic anemia, and hypogammaglobulinemia.
16219353
 MALE Middle Aged
The 5q- syndrome and autoimmune phenomena: report of three cases.
Pinheiro RF, Silva MR, Chauffaille Mde L.
Leuk Res. 2006;30(4):507-10.
Autoimmune manifestations as vasculitis, pyoderma gangrenosum, hemolytic anemia, immune thrombocytopenia, rheumatoid arthritis as well as positive anti-nuclear factor and rheumatoid factor have been reported in 13-30% of MDS patients.
15847658
 FEMALE
Oxaliplatin-induced immune pancytopenia.
Taleghani BM, Meyer O, Fontana S, Ahrens N, Novak U, Borner MM, Salama A.
Transfusion. 2005;45(5):704-8.
Oxaliplatin, a third-generation platinum compound, has been implicated in isolated cases of immune hemolytic anemia and/or immune thrombocytopenia.
15225244
 MIXED_SAMPLE Child
Ceftriaxone causes drug-induced immune thrombocytopenia and hemolytic anemia: characterization of targets on platelets and red blood cells.
Grossjohann B, Eichler P, Greinacher A, Santoso S, Kroll H.
Transfusion. 2004;44(7):1033-40.
Ceftriaxone causes drug-induced immune thrombocytopenia and hemolytic anemia: characterization of targets on platelets and red blood cells.
12675720
 FEMALE Adult
Diclofenac-induced antibodies against RBCs and platelets: two case reports and a concise review.
Meyer O, Hoffmann T, Aslan T, Ahrens N, Kiesewetter H, Salama A.
Transfusion. 2003;43(3):345-9.
Diclofenac has frequently been implicated as the cause of immune hemolytic anemias and less frequently of immune thrombocytopenia.
10942217
 MIXED_SAMPLE Infant, Newborn
Can drugs cause autoimmune thrombocytopenic purpura?
Aster RH.
Semin Hematol. 2000;37(3):229-38.
A wide range of medications can cause life-threatening immune thrombocytopenia (ITP), hemolytic anemia, or neutropenia in sensitive individuals.
10734662
 MALE Child
Immune thrombocytopenia and hemolytic anemia as a presenting manifestation of Hodgkin disease.
Ertem M, Uysal Z, Yavuz G, Gozdasoglu S.
Pediatr Hematol Oncol. 2000;17(2):181-5.
Immune thrombocytopenia and hemolytic anemia as a presenting manifestation of Hodgkin disease.
10455373
 MALE Infant
Immune thrombocytopenia after umbilical cord progenitor cell transplant: response to vincristine.
Dovat S, Roberts RL, Wakim M, Stiehm ER, Feig SA.
Bone Marrow Transplant. 1999;24(3):321-3.
Four months following the transplant, he developed immune thrombocytopenia with hemolytic anemia (Evans syndrome).
8846146
 MALE
Immune thrombocytopenia and hemolytic anemia associated with Hodgkin disease.
Shah SJ, Warrier RP, Ode DL, Lele HE, Yu LC.
J Pediatr Hematol Oncol. 1996;18(2):227-9.
Immune thrombocytopenia and hemolytic anemia associated with Hodgkin disease.
8484132
 MALE Adult
Hypogammaglobulinemia and rheumatic disease.
Lee AH, Levinson AI, Schumacher HR Jr.
Semin Arthritis Rheum. 1993;22(4):252-64.
Autoimmune disorders such as immune thrombocytopenic purpura, immune hemolytic anemia, juvenile rheumatoid arthritis, systemic lupus erythematosus, dermatomyositis, Sjogren's syndrome, essential mixed cryoglobulinemia, chronic active hepatitis, and sarcoidosis have been reported in hypogammaglobulinemic patients.
1287765
 MIXED_SAMPLE Adult
[Lymphoproliferative syndrome with granular lymphocytes of CD8+ phenotype: a clonal pathology with a chronic course].
Pellegrin JL, Merlio JP, Cony-Makhoul P, Ferrer AM, Astier-Gin T, De Mascarel A, Beylot C, Broustet A, Reiffers J, Leng B.
Rev Med Interne. 1992;13(4):261-7.
Splenectomy did not correct neutropenia but allowed the control of hemolytic anemia and auto-immune thrombocytopenia in one case.