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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Main Authors: Agnieszka Giza, Tomasz Stramek, Andrzej Jaworek, Grzegorz Dyduch, Wojciech Jurczak, Aleksander Skotnicki
Format: Article
Language:English
Published: Our Dermatology Online 2016-08-01
Series:Nasza Dermatologia Online
Online Access:http://www.odermatol.com/issue-in-html/2016-3-31/
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spelling 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/
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