Rabbit in the Hat: Newly Diagnosed ITPin Patients with Adrenocortical Carcinoma
Journal Title: Scholars Journal of Medical Case Reports - Year 2017, Vol 5, Issue 9
Abstract
Immune thrombocytopenia (ITP) is a commonly seen acquired bleeding disorders. Particularly, the incidence is recently increasing along with cases detected incidentally. It has been reported in association with non-hematologic malignancies such as breast cancer with a limited number of case reports in the literature. Adrenocortical carcinoma is a rare condition. Here we describe a newly diagnosed ITP resultant after therapy in a patient followed by adrenocortical carcinoma. Even the co-occurrence of these two conditions makes it quite considerable, we find worth sharing as our view about the possible pathophysiological mechanisms.
Authors and Affiliations
Adem Aydin, Gokhan Ozgur, Murat Yildirim, Birol Yildiz, Selim Sayin, Sukru Ozaydin, Musa Barıs Aykan, Cengiz Beyan
An Interesting Case: Congenital Right Adnexal Mass with Diffuse Intraabdominal Ascites
Abstract: Adnexal masses are important at pediatric period; we diagnosed a cystic adnexal mass with diffuse ascites. We aimed to present this case in the light of literature. Keywords: Adnexal mass, Ascites, neonatal, r...
Meckel Gruber Syndrome-An Autopsy Report of a Rare Case
Abstract:Meckel Gruber Syndrome is a rare autosomal recessive disorder characterized by a typical clinical triad of meningo-encephalocele, polycystic kidneys and polydactyly. The worldwide incidence varies from 1 in 1325...
Cross Ectopia: Case Report
Abstract: 65 years old female patient came to the hospital with back pain, hematourea, urine and blood analysis was requested. Then Computerized Tomography Urography (CTU) was requested. Keywords: CTU, CFRE
Medullated retinal nerve fibres a rare association with young ischemic stroke: A Case Report
Abstract: Medullated (Myelinated) retinal nerve fibres(MRNF) are developmental anomaly and occur in less than 1% of the population, however, most of the reported cases of MRNF is with ocular diseases ,systemic associa...
A Case Report of Kartagener Syndrome
Kartagener syndrome/Primary ciliary dyskinesia (PCD) is a rare ciliopathic autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory tract (both lower and upper, sinuses, eust...