Familial Occurrence of Tailgut Cyst Having Possible Association with Currarino Syndrome

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Tailgut cyst accompanied with bony defect.

Retro-rectal cystic hamartoma (tailgut cyst), is an uncommon congenital developmental lesion, generally located in the retro-rectal space. Its diagnosis and approach is challenging because the retropelvic space is not familiar. We report a 51-year-old woman who presented with paresthesia and pain in perianal area. The magnetic resonance image showed high signal intensity on the T1-weighted imag...

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Currarino syndrome

Other names: Currarino triad; ASP (Anal atresia, sacral anomalies, presacral mass); Sacral defect with Anterior Meningocoele Note: Currarino syndrome is a multiple congenital anomalies syndrome characterized by partial agenesis of the sacrum in association with pelvic malformation. Anal atresia and the presence of a pre-sacral mass (teratoma and/or anterior meningocoele) make up the so called C...

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Unusual Perirenal Location of a Tailgut Cyst

The authors describe a case in which a tailgut cyst occurred at an unusual location in a 22-year-old woman referred for abdominal discomfort and urinary frequency. The left abdomen contained a palpable mass, found at imaging studies to be a homogeneous, unilocular and cystic, and anterior to the left kidney. After surgical excision, it was shown to be a tailgut cyst.

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Tailgut cyst prolapsing through the anus.

The tailgut cyst is a rare congenital malformation. It is a remnant of the postanal part of the hindgut, which normally regresses totally during the embryonic period. Most cases are asymptomatic and are diagnosed by incident as a presacral mass, other cases may present with different and unspecific symptoms.1–5 This case presenting as a prolapse through the anus has, to our knowledge, not been ...

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Familial occurrence of the antiphospholipid syndrome.

In a family of four the whole spectrum of antiphospholipid and associated antibodies was present but without evidence of connective tissue disease. All four members had anticardiolipin antibodies; two had a confirmed lupus anticoagulant. Thrombocytopenia was severe in one and associated with a high titre of antiplatelet antibody, while another member was found to have a positive antiglobulin te...

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ژورنال

عنوان ژورنال: The Japanese Journal of Gastroenterological Surgery

سال: 2018

ISSN: 0386-9768,1348-9372

DOI: 10.5833/jjgs.2018.0056