Results 11 to 20 of about 17,105 (224)

Rare pelvic masses: a report of 2 cases [PDF]

open access: yesWaike lilun yu shijian, 2022
Dermoid cyst is congenital benign hamartoma with ectodermal origin and occurs in many parts of the body such as subcutaneous and soft tissue. Most dermoid cysts are solitary and diameter 1 to 4 cm.
PANG Chengyu, HUANG Xunbo, NI Jiaqi, WU Weize
doaj   +1 more source

Dermoid cyst [PDF]

open access: yes, 2023
Dermoid cyst is a benign congenital life-choristoma. This group consists of histologically normal cells arising in an abnormal location and represents childhood's most common orbital attack.
Gjorgieva, Biljana   +5 more
core   +2 more sources

The dirty dozen: Myths in oculoplasty

open access: yesTNOA Journal of Ophthalmic Science and Research, 2020
Medical myths develop when existing beliefs are not challenged. They remind us that we can be mistaken and need to question ourselves. Oculoplasty, a vital branch of ophthalmology, has been of interest to surgeons since olden days.
Akruti Desai, Milind Naik
doaj   +1 more source

Mucinous Cystadenocarcinoma Co-Existing with Mature Cystic Teratoma : A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Co-existence of mucinous cystadenocarcinoma with mature cystic teratoma in the same ovary is very rare. We report a case in a 48- year-old female who presented with left abdominal mass. CT scan revealed a heterogeneous enhancing left ovarian mass lesion.
Prachi Kukreja   +4 more
doaj   +1 more source

Implantation dermoid

open access: yesPan African Medical Journal, 2021
True epidermoid inclusion cysts result from the implantation of epidermal elements in the dermis, and can result from any trauma or surgical procedure. Theoretically, any skin puncture, laceration or incision has the potential to implant epidermal elements into the dermis and subcutaneous tissue, where continued production of keratin and other ...
Surya Besant Natarajan   +1 more
openaire   +3 more sources

Impact of location on resectability and neurological outcome in spinal cutaneous inclusion tumors

open access: yesIndian Spine Journal, 2023
Background: Spinal cutaneous inclusion tumors are extremely rare, accounting for less than 1% of intraspinal tumors. The existing literature is scarce; in last two decades, only eight case series have documented more than 10 patients. We tried to figure
Sundus Ali   +5 more
doaj   +1 more source

Intracranial nasofrontal dermoid cyst and a hair in the nose tip without a sinus tract identified with single‐staged combined approach excision done

open access: yesClinical Case Reports, 2023
Key Clinical Message This is the first reported case of intracranial nasofrontal dermoid without sinus tract, with complete excision done in single‐staged combined approach frontal craniotomy and open rhinoplasty, and satisfactory nasal reconstruction.
Aurora Ka Yue Tam   +7 more
doaj   +1 more source

Acute post‐traumatic dermoid peritonitis: A rare entity

open access: yesClinical Case Reports, 2022
Rupture of ovarian dermoid‐cyst is rare case. We report the case of a woman admitted for acute post‐traumatic abdominal pain due to ruptured ovarian cyst.
Sami Fendri   +7 more
doaj   +1 more source

Non-Ruptured Temporal Lobe Dermoid Cyst Concomitant with Focal Cortical Dysplasia Causing Temporal Lobe Epilepsy—A Case Report and Literature Review

open access: yesBrain Sciences, 2021
Background: Intracranial dermoid cyst is a rare, benign, nonneoplastic tumor-like lesion that could cause seizures, headache, and hydrocephalus. We hypothesized that the temporal lobe dermoid cyst in combination with other factors were causing the ...
Keisuke Hatano   +5 more
doaj   +1 more source

Epiglottan Kaynaklanan Dermoid Kist [PDF]

open access: yes, 2015
WOS:000365356700012PubMed ID:29391978Baş-boyun bölgesinden kaynaklanan dermoid kistler nadir, yavaş büyüyen ve iyi sınırlı benign tümörlerdir. Semptomları, özgün değildir, genellikle lezyonun boyutu ve bulunduğu yere bağlıdır. Epiglottan kaynaklı dermoid
Hilal Yücel   +3 more
core   +1 more source

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