Sharma Ashish, Ali Mohammad, Chauhan Shruti, Singh Smita, Arya Vivek
Department of Rheumatology, Fortis Flt. Lt. Rajan Dhall Hospital, New Delhi, India.
Department of Medicine, Dr. Ram Manohar Lohia Hospital and Post Graduate Institute of Medical Education and Research, New Delhi, India.
Reumatologia. 2019;57(3):178-181. doi: 10.5114/reum.2019.86430. Epub 2019 Jun 28.
Behçet's disease is a multi-systemic vasculitis which is characterized by recurrent oral and genital ulceration with positive pathergy test. These features may also be seen in various hematological malignancies. In patients with leukemia who present with Behçet's disease-like features, it is often difficult to ascertain whether the clinical manifestations are due to leukemia, or there is co-existing Behçet's disease too. The authors report an Indian farmer who presented with clinical features suggestive of Behçet's disease with profound neutropenia. On bone marrow examination he was found to have acute monocytic leukemia (AML-M5). Chemotherapy for leukemia did not relieve his oral and genital ulcers, for which glucocorticoids and colchicine had to be given. So the patient had co-existence of Behçet's disease along with AML-M5, which has never been reported in the literature before.
白塞病是一种多系统血管炎,其特征为复发性口腔和生殖器溃疡且针刺反应阳性。这些特征也可见于各种血液系统恶性肿瘤。在出现类似白塞病特征的白血病患者中,往往难以确定临床表现是由白血病引起的,还是同时存在白塞病。作者报告了一名印度农民,他表现出提示白塞病的临床特征且伴有严重中性粒细胞减少。骨髓检查发现他患有急性单核细胞白血病(AML-M5)。针对白血病的化疗未能缓解他的口腔和生殖器溃疡,为此不得不给予糖皮质激素和秋水仙碱。所以该患者同时存在白塞病和AML-M5,这在以前的文献中从未有过报道。