We report a successful laparoscopic management of an interstitial pregnancy of a 24- year-old single woman, treated by cornuostomy. The patient was first managed with methotrexate treatment. After the 2. methotrexate ...

Hücresel bağışıklık sisteminin baskılandığı kronik bir infeksiyon hastalığına yol açan insan immün yetersizlik virüsü (Human Immunodeficiency Virus, HIV) infeksiyonunun seyri sırasında, bulaşma döneminden ileri aşamasına ...

Mounier-Kuhn Syndrome (MKS) is a rare congenital disease that presents with abnormal enlargement in the central airways. In MKS, tracheomegaly is accompanied by difficulty in expelling recurrent lung infections and ...

INTRODUCTION: Schwannoma is a benign, solitary, and slowly progressive encapsulated tumor originating from the sheath of myelinated nerve fibers. Schwannoma of the salivary gland is a particularly rare form of an extracranial ...

Kemodektoma olarak da bilinen karotis cisim tümörleri (KCT) karotis cisim nöröendokrin dokularından kaynaklanan nadir bir tümördür. Nöral krest kökenlidir. Bu tümörlerin çoğu benign karakterdedir ancak klinik olarak malign ...

Endometriozis, fonksiyonel endometrium bez ve stromanın, uterus boşluğu dışında büyümesi olarak tanımlanır. Sezaryen, histerektomi, apendektomi ve laparoskopi sonrası trokar yerinde; epizyotomi ve amniyosentez sonrasında ...

Human fascioliasis is a rare parasitic disease caused by Fasciola hepatica, affecting mainly the liver and the biliary tract. If not suspected, it may easily be confused with other pathologies that will lead to incorrect ...

Introduction; Absolute pitch (AP) is the term used to denote the cognitive ability to spontaneously and effortlessly identify and vocally produce specific musical tones without a reference note.1 Abnormalities of pitch ...

Background Atypical hemolytic uremic syndrome (aHUS) is associated with defective regulation of the complement pathway. Neurological involvement is the most common extrarenal complication and represents a major cause of ...

Arrhythmogenic right ventricular dysplasia is a heritable disease of the heart muscle characterized by fibrofatty degeneration of cardiomyocytes. Patients present with ventricular arrhythmias or congestive heart failure, ...