scholarly journals Nevus sebaceous of Jadassohn of face with infundibular and keratinous cyst in an adolescent Arab male-a rare case report

2018 ◽  
Vol 6 (3) ◽  
pp. 1033
Author(s):  
Scott Arockia Singh M. ◽  
Paul Raphel ◽  
Sneha Devadas ◽  
Siny Vellukara Sasidharan
Keyword(s):  
Case Report ◽  
Skin Lesion ◽  
Rare Case ◽  
Medical Literature ◽  
Interesting Case ◽  
Malignant Change ◽  
Excision Biopsy ◽  
Rare Case Report ◽  
The Face ◽  
Nevus Sebaceous

Nevus Sebaceous of Jadassohn is rare hamartomatous skin lesion. We report an interesting case of an Adolescent Arab male 18yr old, who presented to us with a velvety plaque of 7cm length in his left preauricular area. Excision biopsy revealed Nevus sebaceous of Jadassohn with infundibular and keratinous cyst. The lesion is present since birth started as a tiny lesion and grown to the current size. No such large sized lesion on the face has ever been reported in the medical literature till date. We advise an early excision as they have strong potential for malignant change.

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

scholarly journals Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature

2015 ◽  
Vol 6 (3) ◽  
pp. 115-117
Author(s):  
Sachin Lal Shilpakar ◽  
Bivek Aryal ◽  
Shyam Thapa Chettri ◽  
Apar Pokharel ◽  
Deepak Paudel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histopathological Examination ◽  
Hair Follicles ◽  
Review Of Literature ◽  
Solitary Lesion ◽  
Biological Potential ◽  
Rare Case Report ◽  
The Face ◽  
Head Neck

ABSTRACT The trichoepithelioma is a benign cutaneous neoplasm which is derived from hair follicles. It is common in the face, but there are only three reports of the solitary occurrence on the nose. It is often not recognized because of its rarity, controversial classification, origin and biological potential. The objective of this paper is to present a case of solitary trichoepithelioma on the nose, histopathological examination and treatment. It should be considered as a differential diagnosis of a solitary lesion of nose which is confused with basal cell carcinoma. The confirmation by histopathological examination is essential. How to cite this article Sah BP, Shilpakar SL, Aryal B, Chettri ST, Pokharel A, Mishra S, Paudel D. Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):115-117.

scholarly journals Psoriasiform Mycosis Fungoides Involving the Face- A Rare Case Report

2021 ◽  
pp. 94-99
Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Punch Biopsy ◽  
Cutaneous T Cell Lymphoma ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Atypical Cells ◽  
The Face

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.

scholarly journals Multicentric Chondrosarcoma Involving the Appendicular Skeleton: A Case Report and Literature Review.

2020 ◽  
Vol 27 (5) ◽  
Author(s):  
V. Aran ◽  
W. Meohas ◽  
A.C. De Sá Lopes ◽  
L. Maciel Cabral ◽  
A. Fortuna Costa ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Medical Literature ◽  
Good Prognosis ◽  
Appendicular Skeleton ◽  
Rare Case Report ◽  
Primary Bone ◽  
Uncommon Case

Chondrosarcomas constitute the 3rd most common primary bone malignancy. These tumours grow slowly and rarely metastasize, usually having a good prognosis after surgery. Among patients registered and treated at the Brazilian National Institute of Traumatology and Orthopedics, an uncommon case of chondrosarcoma was identified in a 63-year-old man, who was diagnosed with multicentric chondrosarcoma of the appendicular skeleton. This example is atypical in the medical literature because multicentric tumours are different from metastatic events, and their frequency in chondrosarcoma is rare. This article therefore provides a rare case report alongside a review of additional cases in the medical literature.

Variant of bohring-opitz syndrome: A rare case report

2021 ◽  
Vol 4 (2) ◽  
pp. 84-86
Author(s):  
Ramesh Choudhary ◽  
Romesh Gauttam ◽  
Vishnu Pansari ◽  
Anand Kumawat
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Medical Literature ◽  
Male Child ◽  
Rare Syndrome ◽  
First Case ◽  
Eventration Of Diaphragm ◽  
Rare Case Report ◽  
Opitz Syndrome

Bohring–Opitz syndrome also known as Opitz C syndrome or Oberklaid–Danks syndrome is a rare syndrome. We are reporting a 2 months old male child with Bohring-Opitz like syndrome with all classical features and eventration of diaphragm   (left side) which has not  been reported yet with this syndrome.  To our knowledge, a total of 23 cases with this syndrome have been reported in the medical literature to date and this is probably the first case report from India. Although there is overlap, a clinical distinction from the Bohring-Opitz syndrome and other syndromes seems possible, and thus a specific causal entity may be postulated.

Erythema Dyschromium Perstans – A Rare Case Report of Dermal Hyperpigmented Skin Lesion

2011 ◽  
Vol 4 (4) ◽  
pp. 413-414
Author(s):  
Dr.Priyadarshini.D Dr.Priyadarshini.D ◽  
◽  
Dr.Satish Araker
Keyword(s):  
Case Report ◽  
Skin Lesion ◽  
Rare Case ◽  
Rare Case Report

Solitary fibrous tumour of the face: a rare case report

2002 ◽  
Vol 55 (1) ◽  
pp. 75-77 ◽  
Author(s):  
Joon Pio Hong ◽  
Yoon Kyu Chung ◽  
Sug-Won Kim ◽  
Tae-Hun Kim ◽  
Kwang-Gil Lee
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Solitary Fibrous Tumour ◽  
Rare Case Report ◽  
The Face

scholarly journals Understanding the “Empty Toe” Phenomenon: A Rare Case Report

2021 ◽  
Vol 111 (2) ◽  
Author(s):  
Nicholas V. DiMassa ◽  
Erik K. Monson ◽  
Kimberly S. Cravey
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Medical Literature ◽  
Review Of The Literature ◽  
Detailed Review ◽  
Soft Tissue Envelope ◽  
Degloving Injury ◽  
Rare Case Report ◽  
Closed Degloving Injury ◽  
Closed Degloving

Closed degloving injury involving a toe represents a rare phenomenon in which the bones of the toe dislocate but the soft-tissue envelope remains intact. It has been described sparingly throughout the medical literature, and outcomes have been poor. This article presents a case report of the unique injury while also investigating trends through a detailed review of the literature.

scholarly journals Duplicated appendix with an acute abdomen in 16 years old female with both appendices inflamed: a rare case report

2020 ◽  
Vol 7 (11) ◽  
pp. 3782
Author(s):  
Shivakumar S. ◽  
Uday Kumar
Keyword(s):  
Case Report ◽  
Severe Pain ◽  
Rare Case ◽  
Incidental Finding ◽  
Iliac Fossa ◽  
Interesting Case ◽  
Ileocaecal Valve ◽  
Rare Congenital Anomaly ◽  
Pain Abdomen ◽  
Rare Case Report

Duplicated appendix is a rare congenital anomaly with incidence of 0.004-0.009% and its mostly an incidental finding on table, when one of them is acutely inflamed and very rarely both of them can be inflamed as in this case. Report a case of young girl who presented with complain of pain abdomen and vomiting in the last 2 days. Clinically patient was diagnosed to have acute appendicitis and on laparoscopy, patient had duplicated appendix one at the ileocaecal valve and the other 2cm away near the caecum with pus and faecolith. Histopathology confirmed appendicitis in the both appendices. Reported about this interesting rare case because even though the incidence of duplicated appendix is too low (0.004-0.009%), should always search for the missed appendix in patients who underwent appendicectomy earlier and complains of severe pain in right iliac fossa. Aim was to report such a rare interesting case and give a small gentle reminder to the surgeons as duplicated appendix even though rare but still a possibility.

scholarly journals Urinary Bladder Leiomyoma: A Rare Case Report

1970 ◽  
Vol 2 (2) ◽  
pp. 70-71
Author(s):  
HU Bhuiyan
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Key Words ◽  
Female Patient ◽  
Rare Case ◽  
Excision Biopsy ◽  
Key Words Urinary Bladder ◽  
Rare Case Report ◽  
Bladder Leiomyoma

A rare case of urinary bladder leiomyoma in a female patient is presented here. A quarter of these cases are asymptomatic only to be diagnosed by ultrasonography. Symptomatic cases are also misleading as in this case. Laparotomy, removal of mass and ultimately histopathology proved the case to be that of a urinary bladder leiomyoma. Ibrahim Med. Coll. J. 2008; 2(2): 70-71 Key Words: Urinary bladder leiomyoma, laparotomy, excision biopsy doi: 10.3329/imcj.v2i2.2943

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