scholarly journals Syringotropic mycosis fungoides responding well to VELP chemotherapy: A case report

2016 ◽  
Vol 11 (6) ◽  
pp. 2254-2258 ◽  
Author(s):  
YANG LUO ◽  
LI ZHANG ◽  
YU-JIAO SUN ◽  
HUA DU ◽  
GUI-LAN YANG
Keyword(s):  
Case Report ◽  
Mycosis Fungoides

scholarly journals Dual CD4/CD8-positive Ichthyosiform Mycosis Fungoides with Lymph Node, Peripheral Blood and Cardiac Involvement: A Case Report

2016 ◽  
Vol 96 (4) ◽  
pp. 564-566 ◽  
Author(s):  
Y Kaku ◽  
A Otsuka ◽  
H Tanizaki ◽  
R Shibuya ◽  
Y Endo ◽  
...  
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Mycosis Fungoides ◽  
Peripheral Blood ◽  
Cardiac Involvement

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 Mycosis fungoides with a dramatic course in a patient with a history of pyoderma gangrenosum – a case report

2017 ◽  
Vol 5 ◽  
pp. 544-554
Author(s):  
Julia Nowowiejska ◽  
Magdalena Świstak ◽  
Anna Baran ◽  
Iwona Flisiak
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Pyoderma Gangrenosum ◽  
History Of

scholarly journals A unique combination of Rosai-Dorfman disease and mycosis fungoides: a case report

2018 ◽  
Vol 6 ◽  
pp. 2050313X1877219 ◽  
Author(s):  
Amanda J Shelley ◽  
Nordau Kanigsberg
Keyword(s):  
Case Report ◽  
T Cell ◽  
Mycosis Fungoides ◽  
Cell Lymphoma ◽  
Cervical Lymphadenopathy ◽  
B Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Unknown Etiology ◽  
Unique Combination ◽  
Rosai Dorfman Disease

Rosai-Dorfman disease (RDD) is a rare histiocytic condition of unknown etiology. Patients with RDD classically present with massive painless cervical lymphadenopathy. However, extra-nodal disease occurs in approximately 40% of cases, with the skin being among the most commonly involved sites. Patients with isolated extra-nodal involvement may present without adenopathy. Reports of RDD occurring in patients with Hodgkin’s lymphoma, and B-cell lymphoma have been published, but there has only been one previous report of RDD in a patient with a T-cell lymphoma. This case report documents a unique combination of RDD and mycosis fungoides (MF), a cutaneous T cell lymphoma. This report also highlights diagnostic challenges in RDD due to the rarity of the condition and its variable presentation.

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