Mycosis fungoides is the commonest type of cutaneous T-cell lymphoma. It is also called as Alibert-Bazin syndrome or granuloma fungoides. Mycosis Fungoides are an uncommon, heterogeneous group of non-Hodgkin lymphomas (NHLs) of T- and B-cell origin where the skin is the primary organ of involvement. Its clinical manifestation includes many clinical and histological forms; such as a patch, plaque, tumor nodules; erythrodermic and poikoilodermous stages which may differ with different stages. The very severe stage of Mycosis fungoides is extracutaneous where any organ may be involved. Only 20 cases of Bulla formation are reported in the literature so far, making it a very rare finding in mycosis fungoides. The majority of reported cases are in adult males. Case presentation: A 45-year-old male, a case of mycosis fungoides IIB, is described in this case report. He presented in an advanced stage of disease with multiple ulcers over the face, bilateral upper limbs, trunk, and back for 6 Months. Conclusion: mycosis fungoides is a very important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides IIB represents a particularly aggressive form of mycosis fungoides. The progression of extracutaneous spread in our patient confirms the advanced stage of the disease. The patient was given topical glucocorticoids, which will show improvement. Still, further awareness of the disease among physicians and pathologists is needed.
Published in | International Journal of Clinical and Experimental Medical Sciences (Volume 8, Issue 4) |
DOI | 10.11648/j.ijcems.20220804.12 |
Page(s) | 56-61 |
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Mycosis Fungoides, Tumor Stage, Skin Nodule, Cutaneous T-Cell Lymphoma
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APA Style
Ufaque Batool, Reema Samo, Rizwan Ali Lakho, Khushboo Jawed, Hassan Jawed. (2022). Mycosis Fungoides: A Clinical Case Report & Review. International Journal of Clinical and Experimental Medical Sciences, 8(4), 56-61. https://doi.org/10.11648/j.ijcems.20220804.12
ACS Style
Ufaque Batool; Reema Samo; Rizwan Ali Lakho; Khushboo Jawed; Hassan Jawed. Mycosis Fungoides: A Clinical Case Report & Review. Int. J. Clin. Exp. Med. Sci. 2022, 8(4), 56-61. doi: 10.11648/j.ijcems.20220804.12
@article{10.11648/j.ijcems.20220804.12, author = {Ufaque Batool and Reema Samo and Rizwan Ali Lakho and Khushboo Jawed and Hassan Jawed}, title = {Mycosis Fungoides: A Clinical Case Report & Review}, journal = {International Journal of Clinical and Experimental Medical Sciences}, volume = {8}, number = {4}, pages = {56-61}, doi = {10.11648/j.ijcems.20220804.12}, url = {https://doi.org/10.11648/j.ijcems.20220804.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijcems.20220804.12}, abstract = {Mycosis fungoides is the commonest type of cutaneous T-cell lymphoma. It is also called as Alibert-Bazin syndrome or granuloma fungoides. Mycosis Fungoides are an uncommon, heterogeneous group of non-Hodgkin lymphomas (NHLs) of T- and B-cell origin where the skin is the primary organ of involvement. Its clinical manifestation includes many clinical and histological forms; such as a patch, plaque, tumor nodules; erythrodermic and poikoilodermous stages which may differ with different stages. The very severe stage of Mycosis fungoides is extracutaneous where any organ may be involved. Only 20 cases of Bulla formation are reported in the literature so far, making it a very rare finding in mycosis fungoides. The majority of reported cases are in adult males. Case presentation: A 45-year-old male, a case of mycosis fungoides IIB, is described in this case report. He presented in an advanced stage of disease with multiple ulcers over the face, bilateral upper limbs, trunk, and back for 6 Months. Conclusion: mycosis fungoides is a very important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides IIB represents a particularly aggressive form of mycosis fungoides. The progression of extracutaneous spread in our patient confirms the advanced stage of the disease. The patient was given topical glucocorticoids, which will show improvement. Still, further awareness of the disease among physicians and pathologists is needed.}, year = {2022} }
TY - JOUR T1 - Mycosis Fungoides: A Clinical Case Report & Review AU - Ufaque Batool AU - Reema Samo AU - Rizwan Ali Lakho AU - Khushboo Jawed AU - Hassan Jawed Y1 - 2022/08/05 PY - 2022 N1 - https://doi.org/10.11648/j.ijcems.20220804.12 DO - 10.11648/j.ijcems.20220804.12 T2 - International Journal of Clinical and Experimental Medical Sciences JF - International Journal of Clinical and Experimental Medical Sciences JO - International Journal of Clinical and Experimental Medical Sciences SP - 56 EP - 61 PB - Science Publishing Group SN - 2469-8032 UR - https://doi.org/10.11648/j.ijcems.20220804.12 AB - Mycosis fungoides is the commonest type of cutaneous T-cell lymphoma. It is also called as Alibert-Bazin syndrome or granuloma fungoides. Mycosis Fungoides are an uncommon, heterogeneous group of non-Hodgkin lymphomas (NHLs) of T- and B-cell origin where the skin is the primary organ of involvement. Its clinical manifestation includes many clinical and histological forms; such as a patch, plaque, tumor nodules; erythrodermic and poikoilodermous stages which may differ with different stages. The very severe stage of Mycosis fungoides is extracutaneous where any organ may be involved. Only 20 cases of Bulla formation are reported in the literature so far, making it a very rare finding in mycosis fungoides. The majority of reported cases are in adult males. Case presentation: A 45-year-old male, a case of mycosis fungoides IIB, is described in this case report. He presented in an advanced stage of disease with multiple ulcers over the face, bilateral upper limbs, trunk, and back for 6 Months. Conclusion: mycosis fungoides is a very important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides IIB represents a particularly aggressive form of mycosis fungoides. The progression of extracutaneous spread in our patient confirms the advanced stage of the disease. The patient was given topical glucocorticoids, which will show improvement. Still, further awareness of the disease among physicians and pathologists is needed. VL - 8 IS - 4 ER -