scholarly journals Large Fibroepithelial Polyp of Vulva

2011 ◽  
Vol 2011 ◽  
pp. 1-2 ◽  
Author(s):  
Mahesha H. Navada ◽  
Poornima Ramachandra B. Bhat ◽  
Sujaya V. Rao ◽  
Nagarathna G.
Keyword(s):  
Rare Case ◽  
Fibroepithelial Polyp ◽  
Rare Occurrence ◽  
Labia Majora ◽  
Polypoidal Growth

A rare case of a large fibroepithelial polyp (FEP) of the vulva is described. The polypoidal growth was 10 cm in its largest diameter, having a long pedicle with features of inflammation secondary to infection, and was found arising from the left labia majora. The patient did not manifest any signs of recurrence following excision. A large and infected FEP of the vulva is a rare occurrence and hence reported.

A Rare Case of Athelia in a Crossbred Cow

2017 ◽  
Vol 12 (3) ◽  
Author(s):  
R. Uma Rani
Keyword(s):  
Dairy Cattle ◽  
Congenital Anomalies ◽  
Rare Case ◽  
Congenital Abnormalities ◽  
Economic Value ◽  
Therapeutic Management ◽  
Rare Occurrence ◽  
Crossbred Cow

The udder is a very important organ and has economic value in dairy cattle. Though highly vulnerable to various disease conditions, e.g. mastitis, congenital anomalies in the udder are of rare occurrence (Dandale et al., 2013). Congenital abnormalities of the mammary system in cows comprise absence of teats, glands, supernumerary teats and imperforate teats. Absence of teat is extremely rare, but isolated cases in which the teats were only represented by slight eminences have been met with (O’ Connor, 1980). Athelia was reported in buffaloes by Sailendra and Sandhya (1998) and Vidyasagar (2009) and in a Japanese black heifer by Ghanem et al. (2011). In the present paper, a rare case of athelia in a Jersey crossbred cow and its therapeutic management by permanent cessation of lactation is reported.

scholarly journals Presternal Thyroglossal Fistula: A Rare Case Report

2013 ◽  
Vol 4 (2) ◽  
pp. 92-94
Author(s):  
Manas Ranjan Rout ◽  
Deeganta Mohanty ◽  
Kamalesh Bobba ◽  
Chakradhar Meta ◽  
Susritha Karri
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Hyoid Bone ◽  
Rare Occurrence ◽  
Thyroglossal Cyst ◽  
Neck Movement ◽  
Sternal Notch ◽  
Rare Case Report ◽  
Congenital Condition ◽  
Head Neck

ABSTRACT Thyroglossal cyst is a congenital condition of the neck where the painless swelling is found in the midline of the neck in between the foramen cecum of tongue base and sternal notch. Condition is common in children. Thyroglossal fistula is either secondary to infection or drainage of a misdiagnosed abscess. Here we are presenting a case of thyroglossal fistula with its opening over the chest and a cord extending from the hyoid bone to the chest causing restriction of the neck movement. Thyroglossal fistula opening in the chest, i.e. over the sternum is very rare and not been reported in any literatures. Treatment of this type of thyroglossal fistula is same as other types, i.e. Sistrunk's operation, where tract along with part of the hyoid bone is to be removed to prevent recurrence. We are reporting this case for its rare occurrence. How to cite this article Rout MR, Mohanty D, Bobba K, Meta C, Karri S. Presternal Thyroglossal Fistula: A Rare Case Report. Int J Head Neck Surg 2013;4(2):92-94.

Trismus and TMJ disorders as first clinical manifestations in an intracranial acquired cholesteatoma

2021 ◽  
Vol 14 (5) ◽  
pp. e242460
Author(s):  
Chiara Copelli ◽  
Domenico Catapano ◽  
Alfonso Manfuso ◽  
Aurelio d’Ecclesia
Keyword(s):  
Hearing Loss ◽  
Temporomandibular Joint ◽  
Otitis Media ◽  
Rare Case ◽  
Clinical Manifestations ◽  
Chronic Otitis Media ◽  
Temporomandibular Joint Disorders ◽  
Intracranial Extension ◽  
Rare Occurrence ◽  
Acquired Cholesteatoma

Intracranial extension of acquired cholesteatoma is a rare occurrence that can develop secondary to trauma, chronic otitis media or acquired aural cholesteatoma. The most commonly observed symptoms are headache and hearing loss. The authors report on a rare case of intracranial cholesteatoma presenting with atypic symptoms: swelling and temporomandibular joint disorders.

scholarly journals A rare case of isolated fallopian tube torsion

2019 ◽  
Vol 8 (11) ◽  
pp. 4570
Author(s):  
Namrita Sandhu ◽  
Sanjay Singh
Keyword(s):  
Fallopian Tube ◽  
Rare Case ◽  
Iliac Fossa ◽  
Imaging Study ◽  
Rapid Diagnosis ◽  
Rare Occurrence ◽  
Adnexal Torsion ◽  
Transabdominal Ultrasonography ◽  
Ready Availability ◽  
Delays In Diagnosis

Isolated torsion of fallopian tube is a rare occurrence. Diagnostic difficulty gets compounded in adolescents because the most commonly used imaging study in young, usually sexually inactive, population is transabdominal ultrasonography which may show normal ovaries, leading clinicians to abandon a diagnosis of adnexal torsion. Other imaging modalities such as CT scan or MRI are less useful for a rapid diagnosis because of the risk of radiation exposure, cost, or lack of ready availability. Delays in diagnosis may increase the likelihood of necrosis of the fallopian tube which would result in salpingectomy as was the case in our case report. Here authors present one such case, wherein one 12 year old girl who attained menarche at 10 years of age presented with acute paraumblical pain and vomiting without any fever, bowel and bladder disturbances. On examination there was tenderness in right iliac fossa. Her USG report was unremarkable. She initially was put-on broad-spectrum antibiotics but without any amelioration of symptoms. Diagnosed as appendicitis by surgeon, she was taken up for laparoscopic appendicectomy. However, it turned out to be a case of fallopian tube torsion, wherein the tube had become gangrenous for which salpingectomy was done.

scholarly journals Tibial Tuberosity Fracture in an Elderly Gentleman: An Unusual Injury Pattern

2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Emma Brown ◽  
Mohammad Taaha Sohail ◽  
Jonathan West ◽  
Benjamin Davies ◽  
Georgios Mamarelis ◽  
...  
Keyword(s):  
Rare Case ◽  
Avulsion Fracture ◽  
Left Knee ◽  
Injury Pattern ◽  
Tibial Tuberosity ◽  
Rare Occurrence ◽  
Review Of The Literature ◽  
Tibial Tuberosity Fracture ◽  
Unusual Injury

Avulsion fracture of the tibial tuberosity is an infrequent injury in adolescents and an extremely rare occurrence in adults. We describe the case of an 86-year-old gentleman presenting after a fall, sustaining injury to the left knee. Radiographs of the left knee showed avulsion fracture of the tibial tuberosity. The purpose of this study was to present a rare case of tibial tuberosity avulsion fracture in an adult, the treatment performed, and the challenges faced. The case is discussed with the review of the literature.

scholarly journals A Rare Case of a Tracheal Fibroepithelial Polyp Treated by an Endobronchial Resection

2008 ◽  
Vol 47 (19) ◽  
pp. 1723-1726 ◽  
Author(s):  
Atsuhito Ushiki ◽  
Masanori Yasuo ◽  
Tsuyoshi Tanabe ◽  
Kazuhisa Urushihata ◽  
Hiroshi Yamamoto ◽  
...  
Keyword(s):  
Rare Case ◽  
Fibroepithelial Polyp

scholarly journals Giant fibroepithelial polyp of the ureter

2017 ◽  
pp. bcr-2016-218999 ◽  
Author(s):  
Mayank Gupta ◽  
Sanjeet Roy ◽  
Cornerstone Wann ◽  
Anu Eapen
Keyword(s):  
Urothelial Carcinoma ◽  
Rare Case ◽  
Histopathological Examination ◽  
Frozen Section ◽  
Polypoid Lesion ◽  
Ureteropelvic Junction ◽  
Fibroepithelial Polyp ◽  
Upj Obstruction

Giant fibroepithelial polyp is a rare cause of ureteric/ureteropelvic junction (UPJ) obstruction. We report a rare case of giant fibroepithelial polyp in a 32-year-old woman involving the whole length of the ureter, reaching up to the UPJ which was clinically and radiologically considered to be urothelial carcinoma. Frozen section showed a polypoid lesion lined by urothelium with no evidence of dysplasia or malignancy. Subsequently, nephroureterectomy was done as there was marked renal hydronephrosis and it was impossible to separate the polyp from the wall of the ureter. Histopathological examination and immunohistochemistry confirmed the diagnosis of giant fibroepithelial polyp, ruling out malignancy.

scholarly journals Aneurysm of an aberrant splenic artery: An extremely rare occurrence

Vascular ◽  
2015 ◽  
Vol 23 (6) ◽  
pp. 637-638 ◽  
Author(s):  
Rohit Bhoil ◽  
Ashwani Tomar ◽  
Sushma Makhaik ◽  
RG Sood ◽  
Nishant Nayyar
Keyword(s):  
Superior Mesenteric Artery ◽  
Mesenteric Artery ◽  
Rare Case ◽  
Splenic Artery ◽  
Surgical Planning ◽  
Medical Literature ◽  
Surgical Intervention ◽  
Rare Occurrence ◽  
Anatomical Variant ◽  
English Medical Literature

An aberrant splenic artery arising from the superior mesenteric artery, also known as the splenomesenteric trunk, is a rare anatomical variant seen in less than 1% of the population and is more common in females. Aneurysms of the splenic artery originating anomalously from the superior mesenteric artery are extremely rare; only 35 cases of aneurysm of an aberrant splenic artery have been described so far in the English medical literature. We report an extremely rare case of aneurysm of aberrant splenic artery in a 28-year-old man in whom the lesion was detected during routine abdominal scanning and confirmed on computed tomography angiography. Aneurysms of an anomalous splenic artery originating from the superior mesenteric artery are extremely rare; however, they are clinically important because possible rupture could be catastrophic. Exploring these variations is important especially if surgical intervention is contemplated. This could greatly affect the surgical planning and avoid injuries to major arteries and organs intraoperatively.

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