Journals / Turkish Journal of Internal Medicine / 2021 / Cilt: 3 - Sayı: Supplement 1

Blastic Plasmacytoid Dendritic Cell Neoplasia: A Rare Case Report

Pages
71–72
Publication Date
2021-03-07
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We report the case we encountered in our clinic and selected CVP as the treatment approach.

📌 3 Key Takeaways

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Objective & Hypothesis:Blastic Plasmacytoid Dendritic Cell Neoplasia (BPDCN) is a rare hematological malignancy whose pathogenesis has not yet been elucidated.
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Key Findings & Data:Skin, bone marrow, and lymph node involvement can be observed, and it is generally seen in men and old adults.
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Conclusion & Impact:We report the case we encountered in our clinic and selected CVP as the treatment approach.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Blastic plasmacytoid dendritic cell neoplasia · cutaneous lymphoma · NK-cell lymphoma

Abstract

Blastic Plasmacytoid Dendritic Cell Neoplasia (BPDCN) is a rare hematological malignancy whose pathogenesis has not yet been elucidated. Skin, bone marrow, and lymph node involvement can be observed, and it is generally seen in men and old adults. Immunohistochemistry (IHC) features of skin and bone marrow biopsy are essential for diagnosis. There are no standardized treatment options for this malignancy, and the prognosis is particularly poor. Although there are no standardized treatment options for this malignancy, multiple agent chemotherapies such as Hyper-CVAD and CHOP can be used. Bone marrow transplantation may be an option for patients with life expectancy. More case reports are required to understand and manage this extremely rare malignancy. We report the case we encountered in our clinic and selected CVP as the treatment approach.

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Cite This Article

SAYDAM, N. H., PINAR, İ. E., ERSAL, T., YALÇIN, C., ORHAN, B., CANDAR, Ö., OZKOCAMAN, V., ÖZKALEMKAŞ, F. (2021). Blastic Plasmacytoid Dendritic Cell Neoplasia: A Rare Case Report. Turkish Journal of Internal Medicine, Cilt: 3 - Sayı: Supplement 1, 71–72. https://ajindex.com/articles/809080

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References (3)

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