Congenital Microgastria Associated With Gallbladder Agenesis, Cholangiopathy and Hepatocellular Fibrosis: A Case Report
نویسندگان
چکیده
منابع مشابه
Congenital agenesis of the gallbladder: a UK case report
Congenital absence of the gallbladder has a reported incidence between 0.013 and 0.075% (Singh et al., Congenital absence of the gallbladder. Surg Radiol Anat 1999; 21: 221-4). With fewer than 500 cases reported in the literature, it is a well-recognised yet rare embryological malformation. Gallbladder agenesis becomes symptomatic in almost a quarter of cases mostly presenting as cholecystitis ...
متن کاملGallbladder agenesis diagnosed intra-operatively: a case report
INTRODUCTION Agenesis of the gallbladder is a rare congenital anomaly occurring in 13 to 65 people of a population of 100,000. The rarity of the condition, combined with clinical and radiologic features that are indistinguishable from those of more common biliary conditions, means that it is rarely diagnosed preoperatively, and patients undergo unnecessary operative intervention. CASE PRESENT...
متن کاملA Case Report of Penis Agenesis (Aphallia)
A neonate was admitted on the second day of birth in the pediatric ward of Kerman medical sciences university No. 1 Hospital, because of abdominal distention and the absence of penis. Physical findings were lethargia, infancy hyporeflexia, abdominal distention without any organomegally, absence of penis, two touchable masses in the scrotum and a hole on scrotum for urine discharge. CBC and e...
متن کاملFamilial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report
BACKGROUND Previous reports of chromosomal aberrations in different forms of congenital diaphragmatic hernia have been described as comprising aneuploidies (for example, trisomy 21), microdeletions, and duplications (for example, monosomy 15q24, 22q11.2). CASE PRESENTATION We describe the first association of a de novo partial tetrasomy 4q35.2 in a father with left-sided, isolated renal agene...
متن کاملCongenital Vomer Agenesis: Report of Two Cases
Introduction: Congenital vomer agenesis is an extremely rare condition in which the vomer bone does not fully develop, which can lead to septal perforation. Case Report: We report two cases with a defect in the vomer bone in the posteroinferior portion of the septum, found accidentally while performing a pre-operative CT scan for nasal obstruction evaluation. They were diagnosed with congenital...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International Journal of Surgery
سال: 2017
ISSN: 1743-9191
DOI: 10.1016/j.ijsu.2017.08.332