Rhee Dukhee, Myssiorek David, Zahtz Gerald, Diamond Alan, Paley Carol, Shende Ashok
Department of Otolaryngology and Communicative Disorders, The Long Island Jewish Medical Center, the Long Island Campus of the Albert Einstein College of Medicine, New Hyde Park, New York 11040, USA.
Laryngoscope. 2002 Feb;112(2):235-7. doi: 10.1097/00005537-200202000-00007.
To present an unusual case of recurrent facial palsy resulting from acute leukemic infiltration of the parotid gland.
Case report.
An 11-year-old boy who had been treated for acute lymphoblastic leukemia (ALL) from 3 to 6 years of age presented with intermittent left facial nerve palsy with concurrent ipsilateral parotid fullness. The initial findings at diagnosis and workup are presented, and the disease progression and resolution with therapy are documented.
The patient had been off therapy when this finding developed. A workup for central and viral etiologies for the facial palsy was unrevealing. Biopsy of the parotid gland demonstrated a lymphoblastic leukemic infiltrate. The patient was placed on a chemotherapy protocol for relapsed leukemia, resulting in complete resolution of the facial palsy.
Isolated facial nerve dysfunction, albeit rare, has been documented as a sign of central nervous system involvement in leukemia, but until now this presentation has not been described in the setting of leukemic relapse presenting with acute infiltration of the parotid gland.
报告一例因腮腺急性白血病浸润导致复发性面瘫的罕见病例。
病例报告。
一名11岁男孩,3至6岁时接受过急性淋巴细胞白血病(ALL)治疗,现出现间歇性左侧面神经麻痹,同侧腮腺饱满。报告了诊断和检查的初始结果,并记录了疾病进展及治疗后的缓解情况。
出现此症状时患者已停止治疗。对面神经麻痹的中枢性和病毒性病因检查均未发现异常。腮腺活检显示淋巴细胞白血病浸润。患者接受了复发性白血病化疗方案,面瘫完全缓解。
孤立性面神经功能障碍虽罕见,但已被记录为白血病中枢神经系统受累的体征,不过迄今为止,在白血病复发伴腮腺急性浸润的情况下尚未有此表现的描述。