scholarly journals Intravascular fasciitis in foot – a rare entity in a rare site

2016 ◽  
Vol 7 (1) ◽  
pp. 81-83
Author(s):  
Ashitha Nanaiah ◽  
Padmapriya Jaiprakash ◽  
Annappa Kudva ◽  
Kanthilatha Pai
Keyword(s):  
Rare Entity ◽  
Rare Site ◽  
Intravascular Fasciitis

scholarly journals Nontraumatic Epidermoid Inclusion Cyst of Vulva in a Young Unmarried Female: A Rare Entity

2014 ◽  
Vol 6 (3) ◽  
pp. 173-175
Author(s):  
Anu Nagpal ◽  
Praveen Mohan
Keyword(s):  
South Asian ◽  
Epidermoid Cyst ◽  
Histopathological Examination ◽  
Rare Entity ◽  
Inclusion Cyst ◽  
Benign Lesions ◽  
Rare Site ◽  
Epidermoid Inclusion Cyst

ABSTRACT Epidermoid inclusion cysts are the most common types of simple dermal epithelial benign lesions, presenting as wellencapsulated subepidermal mobile nodules. They arise on hair-bearing areas but vulva is a rare site. We here report clinical and ultrasonography (USG) findings of a big epidermal nontraumatic inclusion epidermoid cyst at the vulva which was excised and histopathological examination confirmed diagnosis of epidermoid inclusion cyst without any dysplasia. How to cite this article Nagpal A, Mohan P, Kaur T. Nontraumatic Epidermoid Inclusion Cyst of Vulva in a Young Unmarried Female: A Rare Entity. J South Asian Feder Obst Gynae 2014;6(3):173-175.

CYSTADENOMA OF THE PALATE: A RARE SITE FOR A RARE ENTITY

2021 ◽  
Vol 132 (1) ◽  
pp. e35
Author(s):  
AC Perks ◽  
K Martin ◽  
F Domah ◽  
T Bates ◽  
H Anstey
Keyword(s):  
Rare Entity ◽  
Rare Site

scholarly journals Pancreatic kaposiform hemangioendothelioma complicated by Kasabach–Merritt phenomenon: A rare entity

2019 ◽  
Vol 23 (1) ◽  
Author(s):  
Denny Mathew ◽  
Nasreen Mahomed
Keyword(s):  
Differential Diagnosis ◽  
Rare Entity ◽  
Pathological Findings ◽  
Vascular Tumour ◽  
Imaging Studies ◽  
Kaposiform Hemangioendothelioma ◽  
Vascular Neoplasm ◽  
Life Threatening ◽  
Rare Site ◽  
Biochemical Imaging

Primary pancreatic tumours are a rare and unusual entity in children. In this article, we present the case of an 8-month-old girl who presented with obstructive jaundice. The differential diagnosis based on imaging studies was that of a pancreatic vascular neoplasm; however, with the laboratory evidence of Kasabach–Merritt phenomenon (KMP), this prompted the diagnosis of pancreatic kaposiform hemangioendothelioma. A core biopsy of the pancreatic mass was taken at laparotomy and confirmed this diagnosis. The pancreas is an exceedingly rare site of occurrence for this tumour, with only nine cases being published to date. The clinical, biochemical, imaging and pathological findings are discussed to highlight a rare and potentially life-threatening vascular tumour.

scholarly journals What do we know about intravascular fasciitis affecting inferior vena cava? management and report of a case

2017 ◽  
Vol 5 (1) ◽  
pp. 325
Author(s):  
Fernando Mendoza Moreno ◽  
Javier Minguez Garcia ◽  
Maria del Rocio Diez Gago ◽  
Gabriel Olmedilla Arregui ◽  
Benjamin Tallon Iglesias ◽  
...  
Keyword(s):  
Inferior Vena Cava ◽  
Inferior Vena ◽  
Subcutaneous Tissue ◽  
Vena Cava ◽  
Giant Cells ◽  
Histopathological Study ◽  
Rare Entity ◽  
Benign Lesions ◽  
Neoplastic Processes ◽  
Intravascular Fasciitis

Intravascular fasciitis is a rare entity characterized by the proliferation of myofibroblasts and giant cells in relation to small and medium-sized blood vessels. It characterized by a rapid growth and its morphology can simulate other malignant neoplastic processes of more aggressive behavior such as sarcomas. It belongs to a group of benign lesions that affect the subcutaneous tissue and fascia (sometimes to the muscle) sharing characteristics similar to proliferative fasciitis, nodular fasciitis and proliferative myositis. It can sometimes be confused with lesions typical of fibromatosis even. We report a case of a patient with a symptomatic retroperitoneal mass who underwent surgery. The intraoperative findings showed a tumor originating in the inferior vena cava. The histopathological study revealed an intravascular fasciitis.

scholarly journals Frontoethmoidal Extranasopharyngeal Angiofibroma With Orbital Pyocele

2020 ◽  
pp. 014556132097260
Author(s):  
Regi Kurien ◽  
Raghav Mehan ◽  
Lalee Varghese ◽  
Ramesh Babu Telugu ◽  
Meera Thomas ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Frontal Sinus ◽  
Clinical Characteristics ◽  
Postoperative Morbidity ◽  
Radical Surgery ◽  
Vascular Tumors ◽  
Rare Entity ◽  
Sinonasal Mass ◽  
Rare Site ◽  
Extranasopharyngeal Angiofibroma

Significance Statement Extranasopharyngeal angiofibromas (ENA) are rare vascular tumors that do not conform to the clinical characteristics of typical nasopharyngeal angiofibromas. We present the management of an angiofibroma in a rare site, within the frontal sinus with a concomitant orbital pyocele, which was completely excised via an endoscopic approach. ENAs should be considered as a differential diagnosis in patients with sinonasal mass and epistaxis. Awareness of this rare entity will avoid radical surgery thus decreasing postoperative morbidity.

scholarly journals Iliac wing osteochondroma in a 16-year-old boy: a case report

2020 ◽  
Vol 7 (1) ◽  
pp. 171
Author(s):  
Shrihari L. Kulkarni ◽  
Sunil Mannual ◽  
Manjunath S. Daragad ◽  
Sharan H. Girirajaiah
Keyword(s):  
Bone Tumour ◽  
Neurovascular Compression ◽  
Rare Entity ◽  
En Bloc ◽  
Iliac Wing ◽  
Benign Bone Tumour ◽  
Rare Site ◽  
En Bloc Excision ◽  
Bloc Excision ◽  
The Right

<p class="abstract">Osteochondroma is the most common benign bone tumour. Commonly seen in the long bones of the lower extremity. Ilium is a rare site. We present a 16-year-old boy with swelling in the right groin for 8 months. After clinical and radiological evaluation, it was diagnosed as osteochondroma of right iliac wing. Patient underwent en-bloc excision of the lesion and histopathology confirmed the diagnosis. Pelvic osteochondroma is a rare entity but not unusual. Extra periosteal en-bloc excision is the management of choice in patients with cosmetic deformity, neurovascular compression and malignant transformation with very low recurrence rate.</p>

scholarly journals Intradiploic cephalocele: a rare entity at a rare site

2018 ◽  
pp. bcr-2017-223262
Author(s):  
Sunitha V Chakkalakkoombil ◽  
Manchikanti Venkatesh ◽  
Pradeep P Nair ◽  
Umar B Sowkar
Keyword(s):  
Rare Entity ◽  
Rare Site

scholarly journals Isolated vulvo-vaginal Crohn’s disease: case report of the rare entity

2019 ◽  
Vol 6 (4) ◽  
pp. 1400
Author(s):  
Ashwath Narayan Ramji
Keyword(s):  
Crohn’S Disease ◽  
Case Report ◽  
Crohn's Disease ◽  
Healthy Tissue ◽  
Female Genitalia ◽  
Rare Entity ◽  
Intestinal Lesions ◽  
Disease Case ◽  
Rare Site ◽  
Granulomatous Tissue

The vulva is a rare site for extra-intestinal manifestation of Crohn’s disease, and is usually a late feature of severe, fulminant, unrelenting disease. These islands of granulomatous tissue in the female genitalia are considered “metastatic” deposits as they are separated from the intestinal lesions by healthy tissue. Very rarely, Crohn’s disease may manifest first in an extra-intestinal site, without any bowel lesions. In extremely rare cases, the genitalia is the site of isolated primary Crohn’s disease and serves as a harbinger for bowel lesions.

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