Scalp skin primary cutaneous follicle center lymphoma – Case report
Primary cutaneous follicle center lymphoma is an Indolent Cutaneous B-cell Lymphoma responsible for almost 11% of primary cutaneous hematopoietic skin neoplasm. Although PCFCL has excellent prognosis of more than 95% 5 year survival rate it might be a challenge for a clinician because of diagnostic...
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2016-08-01
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doaj-9c3d11eca6424e79acb7945736a553b32020-11-24T23:08:59ZengOur Dermatology OnlineNasza Dermatologia Online2081-93902016-08-017336636810.7241/ourd.20163.100Scalp skin primary cutaneous follicle center lymphoma – Case reportAgnieszka Giza0Tomasz Stramek1Andrzej Jaworek2Grzegorz Dyduch3Wojciech Jurczak4Aleksander Skotnicki5Department of Heamatology, Jagiellonian University College of Medicine, Krakow, PolandDepartment of Heamatology, Jagiellonian University College of Medicine, Krakow, PolandDepartment of Dermatology, Jagiellonian University College of Medicine, Krakow, PolandDepartment of Pathomorphology, Jagiellonian University College of Medicine, Krakow, PolandDepartment of Heamatology, Jagiellonian University College of Medicine, Krakow, PolandDepartment of Heamatology, Jagiellonian University College of Medicine, Krakow, PolandPrimary cutaneous follicle center lymphoma is an Indolent Cutaneous B-cell Lymphoma responsible for almost 11% of primary cutaneous hematopoietic skin neoplasm. Although PCFCL has excellent prognosis of more than 95% 5 year survival rate it might be a challenge for a clinician because of diagnostic difficulties and a need to proceed complete differential diagnosis with systemic follicle center lymphoma. We present a case of a 55-year-old male patient with small, bug bite alike, erythematous, gradually extending lesion on the parietal area of the head. There were no other sign of disease on the skin and no other sides spreading of disease which was confirmed in CT imaging and no other systemic symptoms. After the diagnosis was made course of radical skin lesions 30 Gy radiotherapy were administered. In the follow-up examination skin lesion resolved completely and patient achieved complete remission of the disease.http://www.odermatol.com/issue-in-html/2016-3-31/ |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Agnieszka Giza Tomasz Stramek Andrzej Jaworek Grzegorz Dyduch Wojciech Jurczak Aleksander Skotnicki |
spellingShingle |
Agnieszka Giza Tomasz Stramek Andrzej Jaworek Grzegorz Dyduch Wojciech Jurczak Aleksander Skotnicki Scalp skin primary cutaneous follicle center lymphoma – Case report Nasza Dermatologia Online |
author_facet |
Agnieszka Giza Tomasz Stramek Andrzej Jaworek Grzegorz Dyduch Wojciech Jurczak Aleksander Skotnicki |
author_sort |
Agnieszka Giza |
title |
Scalp skin primary cutaneous follicle center lymphoma – Case report |
title_short |
Scalp skin primary cutaneous follicle center lymphoma – Case report |
title_full |
Scalp skin primary cutaneous follicle center lymphoma – Case report |
title_fullStr |
Scalp skin primary cutaneous follicle center lymphoma – Case report |
title_full_unstemmed |
Scalp skin primary cutaneous follicle center lymphoma – Case report |
title_sort |
scalp skin primary cutaneous follicle center lymphoma – case report |
publisher |
Our Dermatology Online |
series |
Nasza Dermatologia Online |
issn |
2081-9390 |
publishDate |
2016-08-01 |
description |
Primary cutaneous follicle center lymphoma is an Indolent Cutaneous B-cell Lymphoma responsible for almost 11% of primary cutaneous hematopoietic skin neoplasm. Although PCFCL has excellent prognosis of more than 95% 5 year survival rate it might be a challenge for a clinician because of diagnostic difficulties and a need to proceed complete differential diagnosis with systemic follicle center lymphoma. We present a case of a 55-year-old male patient with small, bug bite alike, erythematous, gradually extending lesion on the parietal area of the head. There were no other sign of disease on the skin and no other sides spreading of disease which was confirmed in CT imaging and no other systemic symptoms. After the diagnosis was made course of radical skin lesions 30 Gy radiotherapy were administered. In the follow-up examination skin lesion resolved completely and patient achieved complete remission of the disease. |
url |
http://www.odermatol.com/issue-in-html/2016-3-31/ |
work_keys_str_mv |
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