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Published in 2017 at "Immunologic Research"
DOI: 10.1007/s12026-016-8828-4
Abstract: Concurrent association of idiopathic thrombocytopenic purpura (ITP) and peripheral neuropathy is a rare condition. There are only few case reports published concerning peripheral neuropathy with ITP. One of the etiopathogenetic mechanisms proposed is intraneural hemorrhage,… read more here.
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Published in 2019 at "American Journal of Clinical Pathology"
DOI: 10.1093/ajcp/aqz121.026
Abstract: A 25-year-old female underwent emergent laparoscopic salpingectomy when she presented with an ectopic pregnancy (G1P0). A bone marrow biopsy performed for moderate persistent thrombocytopenia (60-105 K/μL) showed normocellularity, maturing trilineage hematopoiesis, and mildly increased morphologically… read more here.
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Published in 2019 at "Journal of Addiction Medicine"
DOI: 10.1097/adm.0000000000000485
Abstract: : Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disorder defined as low platelet count with normal bone marrow in the absence of other causes of thrombocytopenia. It is caused by autoantibodies binding to several platelet… read more here.
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Published in 2018 at "Medicine"
DOI: 10.1097/md.0000000000010332
Abstract: Rationale: Splenic artery embolization (SAE) is a common procedure in trauma patients with blunt splenic injuries. We report a case of acute ischemic stroke following orthopedic surgery in a patient with post-SAE reactive thrombocytosis. Patient… read more here.
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Published in 2021 at "British Journal of Dermatology"
DOI: 10.1111/bjd.20829
Abstract: Erythromelalgia is a recurrent and paroxysmal syndrome characterized by the clinical triad of bilateral redness, heat, and paroxysmal burning pain, mostly localized on the feet. This disorder can be primary, as a consequence of mutations… read more here.
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Published in 2020 at "Annals of the rheumatic diseases"
DOI: 10.1136/annrheumdis-2020-217694
Abstract: We thank Xie et al for their relevant comments on our recent article in the Annals of Rheumatic Disease entitled ‘Risk of systemic lupus erythematosus in patients with idiopathic thrombocytopenic purpura: a population-based cohort study’.1… read more here.
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Published in 2020 at "Annals of the Rheumatic Diseases"
DOI: 10.1136/annrheumdis-2020-218128
Abstract: We read with great interest the article by Zhu et al .1 It was based on a national study regarding the association between idiopathic thrombocytopenic purpura (ITP) and the subsequent development of systemic lupus erythematosus… read more here.
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Published in 2020 at "Annals of the Rheumatic Diseases"
DOI: 10.1136/annrheumdis-2020-218177
Abstract: We thank Goulielmos et a l1 for their interests on our article entitled ‘Risk of systemic lupus erythematosus (SLE) in patients with idiopathic thrombocytopenic purpura (ITP): a population-based cohort study’.2 Goulielmos et al raised possible… read more here.
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Published in 2018 at "Case Reports in Medicine"
DOI: 10.1155/2018/2096186
Abstract: We present the case of a 19-year-old female with severe hypogammaglobulinemia after having had treatment with rituximab for idiopathic thrombocytopenic purpura requiring intravenous immunoglobulins. She was admitted with the diagnosis of left-sided pneumonia with parapneumonic… read more here.
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Published in 2018 at "Blood"
DOI: 10.1182/blood-2018-99-110642
Abstract: Introduction: Idiopathic thrombocytopenic purpura (ITP) is an acquired platelet disorder that is often caused by antibodies against platelet's antigens. Steroids are effective first therapy for ITP. Steroid-refractory ITP is rare and warrant further investigation and… read more here.
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Published in 2020 at "World Journal of Clinical Cases"
DOI: 10.12998/wjcc.v8.i24.6389
Abstract: BACKGROUND Concomitant ulcerative colitis (UC) and idiopathic thrombocytopenic purpura (ITP) is a rare phenomenon. The management of UC with ITP can be challenging, since a decreased platelet count augments UC. CASE SUMMARY A 24-year-old man… read more here.