Department of Otorhinolaryngology and Head and Neck Surgery, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK
Department of Otorhinolaryngology and Head and Neck Surgery, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
BMJ Case Rep. 2024 Sep 20;17(9):e260059. doi: 10.1136/bcr-2024-260059.
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.
原始细胞性浆细胞样树突细胞瘤(BPDCN)是一种罕见且侵袭性的血液系统恶性肿瘤,通常以皮肤损伤和骨髓累及为特征。我们报告了一位 70 多岁女性的独特病例,她最初因左侧外耳自发性肿胀就诊,类似于血肿,经初始治疗后复发,引发进一步评估。由于患者的髓过氧化物酶(MPO)(p-ANCA)阳性标志物,诊断面临挑战,提示血管炎。皮肤科考虑了各种鉴别诊断,但影像学和检查排除了重要的病理学。类固醇治疗有效,但同时白细胞计数(WCC)急剧增加,促使紧急血液学检查。随后的检查,包括对外耳的皮肤活检和骨髓活检,发现 BPDCN 并发慢性髓单核细胞白血病。该病例突出了具有挑战性的诊断过程,强调了多学科合作的必要性和这种恶性肿瘤独特表现的可能性,扩展了我们对该疾病的认识。