GATA2 缺乏时的侵袭性头颈部鳞状细胞癌

IF 2.3 3区 医学 Q1 OTORHINOLARYNGOLOGY
Brejjette Aljabi, James A Stewart, Kirk Withrow, Carissa M Thomas
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引用次数: 0

摘要

背景:GATA2缺乏症是一种罕见的遗传性疾病,与血液学、感染性和肿瘤并发症相关。我们报告一例GATA2缺乏症患者发展为头颈部侵袭性鳞状细胞癌(SCC),这是这种疾病的非典型表现。方法:一名34岁的西班牙裔男性,非吸烟者,表现为右侧面部外生性肿块。活检显示hpv阴性SCC。计算机断层扫描(CT)显示右侧眼眶周围肿块侵入鼻腔,左侧腮腺对侧肿块延伸至咀嚼间隙。患者接受了广泛的手术,包括右眼眶切除术、全鼻切除术、部分舌切除术、左侧腮腺根治性切除术、左侧下颌髁切除术和双侧颈部切除术。重建包括左颞肌瓣,左颧骨内固定,上颌间固定,以及分阶段的大腿前外侧游离皮瓣用于右侧面部缺损。患者术后左脸手术部位及ALT供体部位出现假单胞菌感染,根据术中培养结果给予抗生素及抗真菌药物治疗。患者的术后过程涉及多种干预措施,以解决并发症和支持恢复。他在手术后迅速发展为双侧局部和区域复发,最终选择姑息治疗。结果:由于该病例为年轻非吸烟患者的侵袭性,结合非典型感染,对免疫缺陷综合征进行了基因检测。他最终被诊断为GATA2缺乏症。结论:该病例强调了在GATA2缺乏的情况下SCC的侵袭性,并强调了在异常恶性肿瘤表现和疑似免疫缺陷患者中进行基因检测的重要性。对患者儿童进行基因检测可以早期诊断GATA2缺乏症,并为通过造血干细胞移植进行治疗性干预提供机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aggressive Head and Neck Squamous Cell Carcinoma in the Setting of GATA2 Deficiency.

Background: GATA2 deficiency is a rare genetic disorder associated with hematologic, infectious, and neoplastic complications. We report a case of a patient with GATA2 deficiency who developed aggressive squamous cell carcinoma (SCC) of the head and neck, an atypical manifestation of this condition.

Methods: A 34-year-old Hispanic male, a nonsmoker, presented with a large, exophytic right facial mass. Biopsy revealed HPV-negative SCC. Computed tomography (CT) showed a right periorbital mass invading the nasal cavity and a contralateral mass in the left parotid extending into the masticator space. The patient underwent extensive surgery, including right orbital exenteration, total rhinectomy, partial glossectomy, left radical parotidectomy, excision of the left mandibular condyle, and bilateral neck dissections. Reconstruction included a left temporalis muscle flap, internal fixation of the left zygoma, intermaxillary fixation, and a staged anterolateral thigh (ALT) free flap for the right facial defect. He developed postoperative Pseudomonas surgical site infections in the left face and ALT donor site and was treated with antibiotics and antifungals based on intraoperative culture results. The patient's postoperative course involved multiple interventions to address complications and support recovery. He developed bilateral local and regional recurrences rapidly after surgery and ultimately elected for palliative care.

Results: Due to the aggressive nature of this case in a young, nonsmoking patient, combined with the atypical infections, genetic testing was performed for immunodeficiency syndromes. He was ultimately diagnosed with GATA2 deficiency.

Conclusion: This case highlights the aggressive nature of SCC in the context of GATA2 deficiency and underscores the importance of genetic testing in patients with unusual malignancy presentations and suspected immunodeficiency. Genetic testing in the patient's children allows for early diagnosis of GATA2 deficiency and provides an opportunity for curative intervention through hematopoietic stem cell transplantation.

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来源期刊
CiteScore
7.00
自引率
6.90%
发文量
278
审稿时长
1.6 months
期刊介绍: Head & Neck is an international multidisciplinary publication of original contributions concerning the diagnosis and management of diseases of the head and neck. This area involves the overlapping interests and expertise of several surgical and medical specialties, including general surgery, neurosurgery, otolaryngology, plastic surgery, oral surgery, dermatology, ophthalmology, pathology, radiotherapy, medical oncology, and the corresponding basic sciences.
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