[PDF] Top 20 Mirizzi syndrome: A rare entity
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Mirizzi syndrome: A rare entity
... hepatic syndrome is the presence of functional sphincter in common hepatic duct that causes stasis and subsequently obstructive ...this Mirizzi syndrome into two types in 1982 (Targarona et ... See full document
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Mirizzi syndrome with an unusual type of biliobiliary fistula—a case report
... Although superior diagnostic modalities, such as MRCP, MDCT, and ERCP have recently emerged, MS with BBF is often diagnosed based on intraoperative findings. Therefore, clinicians need to consider the po- tential ... See full document
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Post laparoscopic cholecystectomy Mirizzi syndrome induced by polymeric surgical clips: a case report and review of the literature
... one rare cause of PCS but it is also well ...postoperative Mirizzi syndrome which requires early management as it can imply an acute and dramatic ...as Mirizzi syndrome caused by ... See full document
7
Extrapelvic endometriosis: a rare entity or an under diagnosed condition?
... Endometrium is one of the most extraordinary tissues of the human body. The ability of endometrium to be im- planted in different tissues and simultaneously to main- tain its functionality is very impressive. It also ... See full document
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Ocular myositis: diagnostic assessment, differential diagnoses, and therapy of a rare muscle disease — five new cases and review ||FREE PAPER||
... the entity of idiopathic orbital infl ammatory syndrome (IOIS), formerly termed orbital ...a rare infl amma- tory disorder of single or multiple extraocular eye ... See full document
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Incidental finding of Zinner syndrome in a Greek military recruit: a case report of a rare clinical entity
... Semen analysis revealed cryptozoospermia (volume < 1 ml, pH 8.0, total sperm count 126 /ml) of obstructive origin. Nevertheless, fertility was not the patient’s primary concern. He declined further management, ... See full document
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Mirizzi syndrome with an unusual aberrant hepatic duct fistula: a case report
... Abstract: Mirizzi syndrome (MS) is a rare complication of chronic cholelithiasis, which is always caused by a calculus in the cystic duct or neck of the gallbladder, resulting in mechanical ... See full document
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Primary renal teratoma: a rare entity
... adulthood [2]. Literature does not reveal a side or gender predilection and almost equal incidence in males and females have been reported [4]. The first reported case of teratoma of kidney was in 1934, when Mc Curdy ... See full document
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Pseudotumoral Colic Tuberculosis: A Rare Pathological Entity
... On other hand, observed anomalies on lab tests like anemia or inflammatory syndrome are non specific. A positive tuberculin skin test (TST) is no confirma- tion of adjacent abdominal TB infection. A plain chest ... See full document
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Sickle Cell Beta Thalassemia: A Rare Entity
... The disorders include sickle cell anemia, the sickle cell beta thalassemia syndromes and hemoglobinopathies in which HbS is in association with abnormal hemoglobin like sickle cell he[r] ... See full document
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Mirizzi syndrome type IV associated with cholecystocolic fistula: a very rare condition- report of a case
... IV Mirizzi syndrome ...for Mirizzi syndrome type IV in order to avoid bile duct injury are two important key points for successful treatment, of these clinical ... See full document
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Avoiding the Trap of Misdiagnosis: Valuable Teaching Points Derived from a Case of Longstanding Popliteal Artery Entrapment Syndrome
... Popliteal artery entrapment syndrome is a rare clinical entity affecting young individuals, causing symptoms of vascular compromise. Delay in diagnosis or misdiagnosis occurs commonly as patients lack ... See full document
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Postpartum atypical haemolytic uremic syndrome: a rare clinical entity
... Atypical HUS accounts for 5-10% of HUS and is a rare life threatening condition as mentioned before. When pregnancy triggers thrombotic microangiopathy, it is referred to as pregnancy associated atypical ... See full document
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Antisynthetase Syndrome in Senegalese Patients: Report of Three Cases
... Antisynthetase syndrome is an original entity and rare au- toimmune myositis and systemic disease, characterized clinically by a wide spectrum of clinical manifestations and the presence of ... See full document
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Low-grade central osteosarcoma in proximal humerus: a rare entity
... a rare case of primary LGCOS affecting the proximal humerus in a young female who finally underwent tumor en bloc resection followed by prosthetic reconstruc- ... See full document
8
A Rare Entity of Angioimmunoblastic T Cell Lymphoma
... AITL is a rare and aggressive T cell malignancy. The clinical symptoms are often vague and nonspecific such as seen in this case. Patients present with predomi- nantly B symptoms such as prolonged fever, ... See full document
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Cerebellar liponeurocytoma – a rare entity: a case report
... In summary, the present study reported a case of cerebellar liponeurocytoma that was successfully treated by total resection without tumor recurrence 15 months after surgery... Conclusio[r] ... See full document
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A Case with Repeated Recurrent Acute Coronary Syndrome due to Pseudoephedrine Use: Kounis Syndrome
... Kounis syndrome include drugs, foods, and environmental agents (insect bite, snakebite, ...Kounis syndrome [3–5], any kind of drug has the potential of inducing allergic reaction and causing Kounis ... See full document
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Liposarcoma of the Nasopharynx: Diagnosis and Management of a Rare Diagnostic Entity
... Provided that nasopharyngeal liposarcomas are exceed- ingly rare, there are very limited reports in the literature with regard to the management of such malignancies [1, 5, 6]. Most therapeutic protocols and ... See full document
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Maxillary Clear Cell Odontogenic Carcinoma - A Rare Entity
... CCOC is a rare odontogenic tumor and very few cases have been reported in the literature. Differentiation from other clear cell lesions is very important. Further studies on clinical, histological and ... See full document
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