Blastic plasmacytoid dendritic cell neoplasm: a rare external ear lesion presenting with leukaemia

被引:0
|
作者
Khan, Hamad Dad [1 ]
Kakar, Sahil [1 ]
Mcclelland, Lisha [1 ]
Hussein, Hayder [2 ]
机构
[1] Univ Hosp Birmingham NHS Fdn Trust, Dept Otorhinolaryngol & Head & Neck Surg, Birmingham, England
[2] Univ Hosp Birmingham NHS Fdn Trust, Dept Haematol, Birmingham, England
关键词
Ear; nose and throat/otolaryngology; Haematology (incl blood transfusion); Oncology; Chemotherapy;
D O I
10.1136/bcr-2024-260059
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive haematological malignancy, typically characterised by cutaneous lesions and bone marrow involvement. We present a unique case of a woman in her 70s, initially seen for a spontaneous swelling on her left external ear resembling a haematoma, which recurred after initial treatment, triggering further evaluation. Diagnostic challenges arose as the patient displayed positive markers for Myeloperoxidase (MPO) (p-ANCA), suggesting vasculitis. Dermatology considered various differential diagnoses, but imaging and tests ruled out significant pathology. Steroid treatment led to improvement, but coincided with a surge in white cell count (WCC), prompting an urgent haematological review. Subsequent investigations, including a punch biopsy of the external ear and a bone marrow biopsy revealed BPDCN concurrent with chronic myelomonocytic leukaemia. This case highlights the challenging diagnostic journey, emphasising the need for multidisciplinary collaboration and the potential for unique BPDCN presentations, expanding our understanding of this malignancy.Summary Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive haematological malignancy, typically characterised by cutaneous lesions and bone marrow involvement. We present a unique case of a woman in her 70s, initially seen for a spontaneous swelling on her left external ear resembling a haematoma, which recurred after initial treatment, triggering further evaluation. Diagnostic challenges arose as the patient displayed positive markers for Myeloperoxidase (MPO) (p-ANCA), suggesting vasculitis. Dermatology considered various differential diagnoses, but imaging and tests ruled out significant pathology. Steroid treatment led to improvement, but coincided with a surge in white cell count (WCC), prompting an urgent haematological review. Subsequent investigations, including a punch biopsy of the external ear and a bone marrow biopsy revealed BPDCN concurrent with chronic myelomonocytic leukaemia. This case highlights the challenging diagnostic journey, emphasising the need for multidisciplinary collaboration and the potential for unique BPDCN presentations, expanding our understanding of this malignancy.Summary Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive haematological malignancy, typically characterised by cutaneous lesions and bone marrow involvement. We present a unique case of a woman in her 70s, initially seen for a spontaneous swelling on her left external ear resembling a haematoma, which recurred after initial treatment, triggering further evaluation. Diagnostic challenges arose as the patient displayed positive markers for Myeloperoxidase (MPO) (p-ANCA), suggesting vasculitis. Dermatology considered various differential diagnoses, but imaging and tests ruled out significant pathology. Steroid treatment led to improvement, but coincided with a surge in white cell count (WCC), prompting an urgent haematological review. Subsequent investigations, including a punch biopsy of the external ear and a bone marrow biopsy revealed BPDCN concurrent with chronic myelomonocytic leukaemia. This case highlights the challenging diagnostic journey, emphasising the need for multidisciplinary collaboration and the potential for unique BPDCN presentations, expanding our understanding of this malignancy.
引用
收藏
页数:4
相关论文
共 50 条
  • [21] Blastic Plasmacytoid Dendritic Cell Neoplasm
    Jain, Akriti
    Sweet, Kendra
    JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2023, 21 (05): : 515 - 521
  • [22] Blastic plasmacytoid dendritic cell neoplasm
    Mejia Urbaez, E.
    Yus Gotor, M. C.
    Hoerndler Argarate, C.
    Salvador Osuna, C.
    Alfaro Torres, J.
    Vicente Arregui, S.
    Rosero Cuesta, D. S.
    Alastuey Aisa, M.
    Torrecilla Idioipe, N.
    Valero Torres, A.
    Munoz Montano, C.
    VIRCHOWS ARCHIV, 2013, 463 (02) : 276 - 276
  • [23] Blastic Plasmacytoid Dendritic Cell Neoplasm
    Chen, Jieping
    Zhou, Jingying
    Qin, Dabing
    Xu, Shuangnian
    Yan, Xiaochu
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (02) : E27 - E29
  • [24] Blastic plasmacytoid dendritic cell neoplasm
    George, S.
    Rider, T.
    Tidbury, H.
    Grace, R.
    Ali, Z.
    Felton, J.
    BRITISH JOURNAL OF DERMATOLOGY, 2015, 173 : 28 - 28
  • [25] Blastic Plasmacytoid Dendritic Cell Neoplasm
    Daniel Kerr
    Ling Zhang
    Lubomir Sokol
    Current Treatment Options in Oncology, 2019, 20
  • [26] Blastic Plasmacytoid Dendritic Cell Neoplasm
    Khoury, Joseph D.
    CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2018, 13 (06) : 477 - 483
  • [27] Blastic plasmacytoid dendritic cell neoplasm: a rare haematological malignancy presenting in the skin with macular purpura
    Lam, M. W.
    Scorer, M.
    BRITISH JOURNAL OF DERMATOLOGY, 2020, 183 : 19 - 19
  • [28] Blastic Plasmacytoid Dendritic Cell Neoplasm in a Young Female: Rare and Challenging
    Modak, Ketan
    Garg, Jeevan Kumar
    Mishra, Deepak Kumar
    Radhakrishnan, Vivek S.
    INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2020, 41 (05) : 761 - 763
  • [29] Blastic plasmacytoid dendritic cell neoplasm. A rare hematodermic malignancy
    Goel, Deepa
    Bhargava, Rahul
    HEMATOLOGY TRANSFUSION AND CELL THERAPY, 2020, 42 (04) : 384 - 386
  • [30] Pediatric Case of Blastic Plasmacytoid Dendritic Cell Neoplasm: A Rare Entity
    Gunduz, Mehmet
    Tugcu, Deniz
    Unuvar, Aysegul
    Yegen, Gulcin
    Buyukbabani, Nesimi
    Sari, Sule Ozturk
    TURKISH JOURNAL OF HEMATOLOGY, 2022, 39 (01) : 68 - 69