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 Atypical Presentation of Mycosis Fungoides- A Rare Case Report

2015 ◽  
Vol 4 (2) ◽  
pp. 62-64
Author(s):  
MA Wahab ◽  
Md Mahabubur Rahaman ◽  
Nehal Warish ◽  
Md Rezaul Quader ◽  
M Hasibur Rahman
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Atypical Presentation ◽  
Cutaneous T Cell Lymphoma ◽  
Papular Eruption ◽  
Clinical Stages ◽  
Rare Case Report ◽  
Late Stages

Commonest cutaneous T cell lymphoma is mycosis fungoides. Clinical stages are patch, plaque, tumor; erythroderma and poikoiloderma. Extracutaneous spread takes place in late stages where any organ may be involved. The majority of reported cases are with typical presentation. A rare case of mycosis fungoides in a 45-year-old male with papular eruption is described. CBMJ 2015 July: Vol. 04 No. 02 P: 62-64

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 Syphilitic Balanitis of Follmann, A Rare Case Report

2021 ◽  
Vol 19 (1) ◽  
pp. 71-73
Author(s):  
Pooja Agarwal ◽  
Ashish Jagati ◽  
Priyanka Vadher ◽  
Malay Chaudhary
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Presentation ◽  
Heterosexual Male ◽  
Primary Syphilis ◽  
Rare Case Report

Syphilitic balanitis of Follmann is a rare presentation of primary syphilis. It can occur before or after the appearance of primary chancre and some time without any associated primary chancre. We are reporting a case of syphilitic balanitis of Follmann, in a 23 years old heterosexual male, who presented with balanitis associated with single indurated lesion over coronal sulcus and few superficial ulcers over prepuce.

Erythema multiforme-like cutaneous lesions in monomorphic epitheliotropic intestinal T-cell lymphoma: a rare case report

2016 ◽  
Vol 44 (2) ◽  
pp. 183-188 ◽  
Author(s):  
Kumpol Aiempanakit ◽  
Chitiarpa Amatawet ◽  
Kanokphorn Chiratikarnwong ◽  
Sauvarat Auepemkiate ◽  
Kanita Kayasut ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Erythema Multiforme ◽  
Rare Case ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Cutaneous Lesions ◽  
Rare Case Report

Cutaneous mantle cell lymphoma: A rare case report

2020 ◽  
Vol 4 (1) ◽  
pp. 61
Author(s):  
Salwa Bano ◽  
Veena Ramaswamy ◽  
BN Tejaswini ◽  
Chaitra Chandrashekar
Keyword(s):  
Case Report ◽  
Mantle Cell Lymphoma ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Mantle Cell ◽  
Rare Case Report

Breast implant‐associated anaplastic large cell lymphoma: A rare case report of lymphoma in the form of a pericapsular solid formation

2019 ◽  
Vol 26 (2) ◽  
pp. 247-251
Author(s):  
Marco Gardani ◽  
Elisa Bellini ◽  
Gabriele Villani ◽  
Nicola Orsi ◽  
Dante Palli
Keyword(s):  
Case Report ◽  
Anaplastic Large Cell Lymphoma ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Breast Implant ◽  
Large Cell ◽  
Rare Case Report ◽  
Large Cell Lymphoma
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