Ali Kabeer, Rashid Tasnuva, Miatech Jennifer, Karan Abhinav, Chandler Zachary, Garcia Gerardo Diaz, Quan W J R
Department of Medicine, University of Florida College of Medicine: Jacksonville, Jacksonville, Florida, USA.
Department of Pathology, University of Florida College of Medicine: Jacksonville, Jacksonville, Florida, USA.
Case Rep Oncol Med. 2025 Sep 6;2025:3563591. doi: 10.1155/crom/3563591. eCollection 2025.
Systemic mastocytosis (SM) is a rare blood disorder characterized by the clonal proliferation of mast cells in tissues. Mast cells release various vasoactive mediators, including histamine, leukotrienes, prostaglandins, platelet-activating factors, and cytokines such as tumor necrosis factor. Clinical manifestations can range from mild itching to severe distributive shock. In some rare cases, mastocytosis is associated with other blood disorders, such as systemic mastocytosis with associated hematologic neoplasm (SM-AHN). Almost all cases of SM exhibit a KIT point mutation. We report a rare case of KIT-negative SM associated with acute myeloid leukemia. Historically, AML has been associated with a poor prognosis, and further research is needed to understand the prognosis of SM associated with AML. In this particular case, the patient underwent induction chemotherapy with azacitidine and venetoclax, and a follow-up bone marrow biopsy showed a reduction in mastocytosis without complete hematologic recovery. The authors aim to present this case as an example of the complex nature of SM and its diverse clinical presentations.
系统性肥大细胞增多症(SM)是一种罕见的血液疾病,其特征是组织中肥大细胞的克隆性增殖。肥大细胞释放多种血管活性介质,包括组胺、白三烯、前列腺素、血小板活化因子以及细胞因子如肿瘤坏死因子。临床表现从轻度瘙痒到严重的分布性休克不等。在一些罕见情况下,肥大细胞增多症与其他血液疾病相关,如伴有相关血液肿瘤的系统性肥大细胞增多症(SM-AHN)。几乎所有SM病例都存在KIT点突变。我们报告了一例罕见的与急性髓系白血病相关的KIT阴性SM病例。从历史上看,急性髓系白血病的预后较差,需要进一步研究以了解与急性髓系白血病相关的SM的预后。在这个特定病例中,患者接受了阿扎胞苷和维奈克拉的诱导化疗,后续骨髓活检显示肥大细胞增多症有所减轻,但血液学未完全恢复。作者旨在将此病例作为SM复杂性质及其多样临床表现的一个例子进行展示。