Results 71 to 80 of about 12,816 (223)

Idiopathic thrombocytopenic purpura and hyperthyroidism : A case report [PDF]

, 1977
The original publication is available at http://www.samj.org.zaA case of immune thrombocytopenic purpura (ITP) and hyperthyroidism is presented. The treatment of refractory ITP with immunosuppressive agents is briefly considered.
Getaz, E. P., Staples, W. G.
core  

Open heart surgery for cyanotic heart disease in a child with immune thrombocytopenic purpura:a case report

Indian Journal of Anaesthesia, 2007
Acute immune thrombocytopenic purpura in children, though a benign self limiting condition, at times complicated with life threatening haemorrhage. In spite of bleeding episode it is inevitable that surgical procedure will be performed on patients with ...
Minati Choudhury, Nirvik Pal, Usha Kiran
doaj  

Severe thrombocytopenia in patients with idiopathic pulmonary arterial hypertension provided several strategies for lung transplantation

Pulmonary Circulation, 2020
While the prognosis of idiopathic pulmonary arterial hypertension has improved significantly due to newer medications, lung transplantation remains a critical therapeutic option for severe pulmonary arterial hypertension.
Takayuki Kobayashi, Ayako Shigeta, Jiro Terada, Nobuhiro Tanabe, Toshihiko Sugiura, Seiichiro Sakao, Kohei Taniguchi, Takahiro Oto, Koichiro Tatsumi   +8 more
doaj   +1 more source

Idiopathic Thrombocytopenic Purpura (ITP): A Case Report

, 2018
Idiopathic thrombocytopenic purpura (ITP) is an anomalous decrease in the number of platelets with obscure etiologic causes. Clinical signs primarily include muco-cutaneous i.e. Petechia, purpura, ecchymosis.
Neha Jajodia, Priya Kandpal, Subha Laksmi, Santosh Agarwal   +3 more
core   +1 more source

Recurrent Acute Myocardial Infarction in Patients with Immune Thrombocytopenic Purpura

Journal of Patient-Centered Research and Reviews, 2014
Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura, is an acquired immune-mediated disease of adults and children characterized by a transient or persistent decrease of platelets and, depending upon the degree of ...
Fengyi Shen, Tonga Nfor, Tanvir Bajwa
doaj   +1 more source

Use of romiplostim in pregnancy for refractory idiopathic thrombocytopenic purpura: Two case reports with maternal and fetal outcomes and literature review

, 2018
Idiopathic thrombocytopenic purpura is a relatively rare complication occurring in pregnancy, with the potential for serious maternal and fetal outcomes.
John Svigos, David M Ross, Simon Kane, Mark R Morton, Su J Chua   +4 more
core   +1 more source

Idiopathic thrombocytopenic purpura. Clinical case

Zaporožskij Medicinskij Žurnal, 2015
Aim. To draw the attention of physicians - internists to the problem of thrombocytopenia and hemorrhagic vasculitis. To describe the clinical case of idiopathic thrombocytopenic purpura, features of diagnostics and treatment of this disease at various ...
V. V. Syvolap , Ye. V. Novikov, O. G. Onishko   +2 more
doaj   +1 more source

Diabetes mellitus de tipo I y púrpura trombocitopénica inmunitaria en una niña

Medisan
Se detalla el caso clínico de una paciente de 11 años de edad, con antecedentes de diabetes mellitus de tipo I, que comenzó a presentar manchas de color rojo oscuro en la piel (similares a moretones) en brazos, frente y piernas desde hacía 3 meses.
José Raúl Zaldívar Ochoa, Alejandro Rodríguez Carballo, Maiyelín Quesada Cortés, Ana Navarro Lautén   +3 more
doaj   +2 more sources

A Remarkable Improvement of Patients with Idiopathic Thrombocytopenic Purpura after appendectomy including Carcinoid tumor

Iranian South Medical Journal, 2011
The assistance of chronic idiopathic thrombocytopenic purpura and appendiceal carcinoid tumor is so rare and has not been reported before .we present here in a 11 year old boy that is the known case of chronic idiopathic thrombocytopenic purpura (with ...
Hamidreza Alizadeh-Otaghvar, Saeedeh Firoozbakht, Sahar Montazeri, Samaneh Khazraie, Marjan Bani Ahmad, Maryam Hajiloo   +5 more
doaj  

Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema [PDF]

, 2015
Hereditary angioedema is a rare, but potentially life-threatening genetic disorder that results from an autosomal dominant trait. It is characterized by acute, recurrent attacks of severe local edema, most commonly affecting the skin and mucosa. Swelling
Andersen, Michelle Fog, Anette Bygum, Michelle Fog Andersen, Bygum, Anette; id_orcid   +3 more
core   +1 more source