A case report: A rare presentation of mandibular condylar fibrous dysplasia

2019 ◽  
Vol 16 (1) ◽  
pp. 70
Author(s):  
MoshoodFolorunsho Adeyemi ◽  
MoninuolaAdebusola Ernest ◽  
Ehigie Igben ◽  
HabibAyodeji Adeyemi
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Rare Presentation

scholarly journals Prevention of pathological fracture in fibrous dysplasia of proximal femur in a 24-year-old female a rare presentation - a case report

2021 ◽  
Vol 7 (6) ◽  
pp. 1238
Author(s):  
Amit Supe ◽  
Jayesh Mhatre ◽  
Nihar Modi
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Pathological Fracture ◽  
Medical Literature ◽  
Favourable Outcome ◽  
Endocrine Dysfunction ◽  
Rare Presentation ◽  
Café Au Lait Spots ◽  
Hip Screw

<p class="abstract">Fibrous dysplasia (FD) was historically mentioned in the medical literature in 1938 by Dr. Lichtenstein and in 1942 by Dr. Lichtenstein and Jaffe. The term Jaffe-Lichtenstein syndrome is sometimes used synonymously with monostotic FD or to denote cases of polyostotic FD with café au lait spots, but no endocrine dysfunction. Our case is a 24-year-old female, housewife presented to our hospital with a complaints of right hip pain and backache with difficulty in walking of 6 months duration. She had dull aching pain which increased in intensity with the course of time, there was no radiation, but was aggravated by movements. She was managed with dynamic hip screw along with curettage of the lesion and bone graft, after 9 months of follow up, she had no pain over her hip and there was calcification over the previous lesion, our patient had a very favourable outcome.</p>

Fibrous Dysplasia of the Clivus: Case Report

Skull Base ◽  
2007 ◽  
Vol 17 (S 1) ◽  
Author(s):  
Kerem Bikmaz ◽  
Celal Iplikcioglu ◽  
Cem Dinc ◽  
Erdinc Ozek
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia

Pathological Fractures from Craniocervical Polyostotic Fibrous Dysplasia Treated with Percutaneous Vertebroplasty: Case Report

Skull Base ◽  
2007 ◽  
Vol 17 (S 1) ◽  
Author(s):  
Mirza Baig ◽  
David Dang ◽  
Gregory Christoforidis ◽  
Antonio Chiocca ◽  
Gabriel Josue
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Percutaneous Vertebroplasty ◽  
Polyostotic Fibrous Dysplasia ◽  
Pathological Fractures

Fibrous dysplasia of maxilla: An unusual case report

2016 ◽  
Vol 3 (1) ◽  
pp. 1-4
Author(s):  
Leena James ◽  
Tejavathi Nagaraj ◽  
Haritma Nigam ◽  
Yogesh
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Unusual Case ◽  
Unusual Case Report

scholarly journals A Case of Epidermal Cyst with Underlying Lipoma on the Back: A Rare Presentation

2021 ◽  
pp. 171-175
Author(s):  
Yuichi Kurihara ◽  
Koji Kawamura ◽  
Masutaka Furue
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Skin Tumors ◽  
Epidermal Cyst ◽  
Rare Presentation

The coexistence of epidermal cysts and lipomas at the same site is extremely rare, although epidermal cysts and lipomas are both common benign skin tumors. We present a rare case of an epidermal cyst with underlying lipoma on the back. This case report may simply be a result of coincidence, but the possibility of underlying subcutaneous tumors should be considered before epidermal cyst surgery.

Case Report and Literature Review of Nodular Hidradenoma, a Rare Adnexal Tumor That Mimics Breast Carcinoma, in a 20-Year-Old Woman

2019 ◽  
Vol 50 (3) ◽  
pp. 320-325
Author(s):  
Vanya Jaitly ◽  
Richard Jahan-Tigh ◽  
Tatiana Belousova ◽  
Hui Zhu ◽  
Robert Brown ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Breast Carcinoma ◽  
Literature Review ◽  
Sweat Glands ◽  
Rare Presentation ◽  
Adnexal Tumor ◽  
Nodular Hidradenoma ◽  
Growing Mass ◽  
Uncommon Tumor

Abstract Nodular hidradenoma is an uncommon cutaneous adnexal tumor arising from sweat glands. In the skin, it usually presents as a solitary dermal nodule; excision is curative in most cases. In rare instances, it may present as a breast mass and can mimic breast carcinoma clinically and radiologically, causing diagnostic dilemmas for the treating physician and pathologist. Herein, we discuss a case of nodular hidradenoma in a 20-year-old Hispanic woman as a rapidly growing mass in the breast that mimicked breast carcinoma. We discuss the rare presentation of this uncommon tumor and the differential diagnosis of this entity, as well as the results of our literature review on the topic.

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