Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a malignancy with high frequency of skin involvement. A 39-year-old Caucasian female was suffering from weakness, myalgia, and skin eruption, which appeared during treatment of chlamydiosis with antibiotics in July 2016. Based on clinical prese...

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Main Authors: Anastasiia Kolerova, Irina Sergeeva, Julia Krinitsyna, Natalia Pronkina, Svetlana Sizikova, Pavel Filimonov, Irina Kryuchkova
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Indian Journal of Dermatology
Subjects:
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2020;volume=65;issue=3;spage=217;epage=221;aulast=Kolerova
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spelling doaj-2fd28b86e7774d859937047d63e1f43a2020-11-25T02:25:37ZengWolters Kluwer Medknow PublicationsIndian Journal of Dermatology0019-51541998-36112020-01-0165321722110.4103/ijd.IJD_235_18Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overviewAnastasiia KolerovaIrina SergeevaJulia KrinitsynaNatalia PronkinaSvetlana SizikovaPavel FilimonovIrina KryuchkovaBlastic plasmacytoid dendritic cell neoplasm (BPDCN) is a malignancy with high frequency of skin involvement. A 39-year-old Caucasian female was suffering from weakness, myalgia, and skin eruption, which appeared during treatment of chlamydiosis with antibiotics in July 2016. Based on clinical presentation, laboratory investigations, and histological examination of skin and bone marrow biopsy, a diagnosis of BPDCN with the involvement of skin, bone marrow, and central nervous system was made. The patient was put on acute lymphoblastic leukemia-like chemotherapy and achieved complete remission in November 2016, the eruption regressed. In January 2017, allogeneic bone marrow transplantation from matched sibling was performed. Since May 2017, the cutaneous relapse with loss of CD56 expression has developed. This clinical case demonstrates the importance of laboratory tests. Histological examination helps to clarify a diagnosis of cutaneous lymphoma; however, a specific type of lymphoma needs immunohistochemical analysis. In our case, BPDCN at the initial stage presented like a systemic vasculitis.http://www.e-ijd.org/article.asp?issn=0019-5154;year=2020;volume=65;issue=3;spage=217;epage=221;aulast=Kolerovablastic plasmacytoid dendritic cell neoplasmcutaneous lymphomacutaneous oncology
collection DOAJ
language English
format Article
sources DOAJ
author Anastasiia Kolerova
Irina Sergeeva
Julia Krinitsyna
Natalia Pronkina
Svetlana Sizikova
Pavel Filimonov
Irina Kryuchkova
spellingShingle Anastasiia Kolerova
Irina Sergeeva
Julia Krinitsyna
Natalia Pronkina
Svetlana Sizikova
Pavel Filimonov
Irina Kryuchkova
Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
Indian Journal of Dermatology
blastic plasmacytoid dendritic cell neoplasm
cutaneous lymphoma
cutaneous oncology
author_facet Anastasiia Kolerova
Irina Sergeeva
Julia Krinitsyna
Natalia Pronkina
Svetlana Sizikova
Pavel Filimonov
Irina Kryuchkova
author_sort Anastasiia Kolerova
title Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
title_short Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
title_full Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
title_fullStr Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
title_full_unstemmed Blastic plasmacytoid dendritic cell neoplasm: Case report and literature overview
title_sort blastic plasmacytoid dendritic cell neoplasm: case report and literature overview
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Dermatology
issn 0019-5154
1998-3611
publishDate 2020-01-01
description Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a malignancy with high frequency of skin involvement. A 39-year-old Caucasian female was suffering from weakness, myalgia, and skin eruption, which appeared during treatment of chlamydiosis with antibiotics in July 2016. Based on clinical presentation, laboratory investigations, and histological examination of skin and bone marrow biopsy, a diagnosis of BPDCN with the involvement of skin, bone marrow, and central nervous system was made. The patient was put on acute lymphoblastic leukemia-like chemotherapy and achieved complete remission in November 2016, the eruption regressed. In January 2017, allogeneic bone marrow transplantation from matched sibling was performed. Since May 2017, the cutaneous relapse with loss of CD56 expression has developed. This clinical case demonstrates the importance of laboratory tests. Histological examination helps to clarify a diagnosis of cutaneous lymphoma; however, a specific type of lymphoma needs immunohistochemical analysis. In our case, BPDCN at the initial stage presented like a systemic vasculitis.
topic blastic plasmacytoid dendritic cell neoplasm
cutaneous lymphoma
cutaneous oncology
url http://www.e-ijd.org/article.asp?issn=0019-5154;year=2020;volume=65;issue=3;spage=217;epage=221;aulast=Kolerova
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