Extrarectal mass: A tailgut cyst

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چکیده

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A Tailgut Cyst—Cystic Mass Diagnosed by Prenatal Ultrasonography

Tailgut cysts are congenital lesions found in the presacral space. These have been mainly identified in adults and are rare in children, especially neonates. Here, we present the case of a neonate with a presacral cystic mass detected by prenatal ultrasonography that was diagnosed as a tailgut cyst after postnatal surgical removal. When a presacral cyst is encountered, tailgut cyst should be co...

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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 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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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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A rare case of carcinoid tumor in a tailgut cyst

Tailgut cysts are rare congenital lesions that arise from the failure of regression of the embryological tailgut. We report a case of neoplastic transformation of tailgut cyst to carcinoid tumor which is exceedingly uncommon.

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ژورنال

عنوان ژورنال: Journal of the Royal Society of Medicine

سال: 2000

ISSN: 0141-0768,1758-1095

DOI: 10.1177/014107680009300214