A Rare Anomalous Case of Absence
نویسندگان
چکیده
A rare anomaly, in which the celiac artery was not present, that is, the left gastric, the splenic and the common hepatic arteries arose independently from the abdominal aorta in that order, was found in an 80-year-old Japanese female among cadavers for student dissection. Such a case was not described in Adachi's classification (1928) of the variations of the celiac artery, but seemed to belong to type V of Morita's classification (1935). This type was a rare, valuable and embryologically primitive pattern, which was suggested by Morita as typus primitivus, and has been reported a few times.
منابع مشابه
Clinical Implications of Congenital Absence of Circumflex Coronary Artery
Introduction: Coronary artery anomalies are rare clinical entities reported in 0.6% to 5.6% of diagnostic coronary angiographies. Anomalous origins of coronary arteries from distal segments are rarely reported. Presented herein is a coronary anomaly in which the circumflex artery (CX) originated as a continuation of the posterolateral branch of the right coronary artery (RCA) w...
متن کاملCongenital Absence of Left Circumflex Coronary Artery
Congenital absence of left circumflex artery is a rare congenital anomaly of the coronary arteries. The prevalence of the anomaly in different studies ranges from 0.6% to 1.3%. Of these, 80% are benign and asymptomatic and 20% are clinically important. We report a 56-year-old man presented with acute resting chest pain who was diagnosed as having acute anterolateral infarction accompanied by el...
متن کاملDifferent Presentation of Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery in Adults: Case Reports
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation. We report three cases of ALCAPA who survived to adulthood. The first case was a 51-year-old woman who complained of typical chest pain that was diagnosed with ALCAPA using cardiac catheterization and coronary computed tomographic angiography (CTA). The second case was a 30-...
متن کاملP-37: The Ejaculatory Duct Ectopically InvadingTowards the Bladder with Multiple CongenitalMalformations of the Homolateral UrogenitalSystem: A Report of a Rare Case and an EmbryologicalReview
Background: To report a rare case of a left ejaculatory duct that allotropically protrudes or invades towards the left vesicle triangular area with its dead end. Materials and Methods: The patient simultaneously exhibited multiple congenital malformations of the homolateral urogenital system, such as the absence of a left kidney, the dysplasia and allotopia of the left seminal vesicle, the abse...
متن کاملRare cavernous haemangioma of the oral cavity with numerous phleboliths
Hemangiomas are tumors of blood vessels identified by rapid endothelial cell proliferation in early infancy followed by involution over time. All other abnormalities are malformations resulting from anomalous development of vascular plexuses. This lesion in the oral cavity is not common. Despite its benign origin and behaviour, it is always of clinical importance to the dental profession and re...
متن کاملA case report of partial bilateral hind limb adactyly in a male lamb
Hemimelia as a congenital anomaly is a failure of development of extremities formation in embryonic period. This anomaly is defined as complete absence of the part of extremities and different forms were explained for hemimelia. Adactyly is an alternative name for transverse hemimelia and is a rare disorder in the most of animal species. A two months old male lamb with normal vital signs was re...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2012