نتایج جستجو برای: complex choristoma

تعداد نتایج: 784099  

2016
Hosny Ahmed Zein M. Tarek A. Moustafa

Ectopic cilia (EC) are a very rare condition with only few cases reported in literature. Many associations were seen with ectopic cilia which include distichiasis, choristoma and aberrant lacrimal gland, hypochromic nevus, atopic eczema and others. We are reporting a case of an 11-year-old girl with isolated left upper lid ectopic cilia, which was confirmed by surgical removal and histopatholog...

Journal: :Australian and New Zealand Journal of Ophthalmology 1975

Journal: :journal of minimally invasive surgical sciences 0
julian klaus smyth faculty of medicine, the university of sydney, camperdown, australia; faculty of medicine, the university of sydney, camperdown, p. o. box: 2139, australia. tel: +61-297679782 kheng seong ng academic colorectal unit, concord hospital campus, university of sydney, concord, australia elizabeth caroline sinclair douglas hanly moir pathology, 14 giffnock ave, macquarie park, nsw, 2113, australia samuel kuo department of upper gastrointestinal and hepatobiliary surgery, macquarie university, north ryde, australia

conclusions we outlined its biliary drainage and blood supply, as well as our surgical approach, which may be a guide to surgeons who encounter hepatic choristomas in their clinical practice. introduction hepatic choristomas, defined as completely separated ectopic liver tissue, are rare. they are most commonly found adjacent to the gallbladder. details of their anatomy, such as blood supply an...

2016
Mohammad Sharifi Maral Namdari

PURPOSE To report a rare case of encephalocraniocutaneous lipomatosis (ECCL) presented with characteristic multiple organ involvement. METHODS A 7-day-old white Iranian girl was referred with ocular, skin and brain abnormalities. RESULTS The findings of nevus psiloliparus, eyelid choristoma and intracranial lipoma were consistent with ECCL. CONCLUSION Since the skin and ocular manifestati...

Journal: :International Journal of Otolaryngology and Head & Neck Surgery 2022

Hairy polyp is an unusual, rare benign developmental malformation of neonates and infants. Embryologically, they are lesions containing both ectodermal mesodermal origin. Based on size, location the lesion, can produce symptoms such as feeding difficulties, airway obstructions, apneic episodes. We present a case hairy at Oro/Nasopharynx causing difficulties immediately after birth. explained mo...

Journal: :The Medical journal of Malaysia 2005
R N Dipak P Kailesh M J Sherry C Anindya

Neonatal stridor resulting from intrinsic or extrinsic aberration in the upper respiratory tract often poses not only a diagnostic problem, but also a difficult airway and a dilemma as to the necessity / timing of surgical intervention. A 45 day old female child with increasing stridor since birth was managed by emergency intubation and CT scan followed by excision biopsy of the cystic left sid...

Journal: :Japanese Journal of Oral & Maxillofacial Surgery 1990

Journal: :Journal of Marine Medical Society 2018

Journal: :Journal of Indian Association of Pediatric Surgeons 2017

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