Retrorectal Cystic Hamartoma (Tailgut Cyst): Report of a Case and Review Of Literature
نویسندگان
چکیده
منابع مشابه
[Retrorectal cystic hamartoma (tailgut cyst): an uncommon cause of recurrent abdominal pain.]
Retrorectal cystic hamartomas are rare congenital lesions that arise from aberrant remnants of the postanal gut. Most of them appear as asymptomatic lesions in middle-aged women but they can manifest with nonspecific symptoms such as abdominal or pelvic pain, constipation or diarrhoea, genitourinary symptoms, etc. Due to their anatomical position and variable presentation these lesions are ofte...
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A 50-year-old man presented with a 6-week history of lumbosacral back pain and altered bowel habit without hematochezia. Abdominopelvic computed tomography (CT) revealed a 5-cm rectal mass with obliteration of the fat plane between the mass and the tip of the coccyx that was interpreted as representing a neoplasm(●" Fig.1a). Followinganormal digital rectal exam, colonoscopy revealed a subtle po...
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Hamartoma of the breast is a rare benign breast lesion which is unfamiliar to most clinicians, although the mammographic features are usually characteristic. Hamartomas are composed of ducts, lobules, fat and fibrous tissue. These benign lesions are likely to be increasingly diagnosed because of routine screening and hence clinical awareness is paramount to prevent these lesions from being ...
متن کاملSurgical management of a retro-rectal cystic hamartoma (tailgut cyst) using a trans-rectal approach: a case report and review of the literature
INTRODUCTION Retro-rectal cystic hamartoma (tailgut cyst) is a rare congenital developmental lesion arising from post-natal primitive gut remnants in the retro-rectal space. The rarity of the lesion and its anatomical position usually leads to difficulty in diagnosis and surgical management. Complete surgical resection remains the cornerstone of treatment. A dozen or so surgical approaches have...
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Folliculosebaceous Cystic Hamartoma (FSCH) is a cutaneous hamartoma comprised of follicular, sebaceous and mesenchymal elements, and usually occurring during adulthood. Congenital and childhood presentations of this lesion are exceedingly rare. We describe herein a case of congenital FSCH on the midline and posterior region of the neck in a 1-year-old male infant and highlight the clinico...
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ژورنال
عنوان ژورنال: Indian Journal of Surgery
سال: 2012
ISSN: 0972-2068,0973-9793
DOI: 10.1007/s12262-012-0633-2