Aggressive Cutaneous Squamous Cell Carcinomas Following Treatment for Graft-versus-Host Disease: A Case Report and Review of Risk Factors

IF 1.6 Q3 DERMATOLOGY Dermatopathology Pub Date : 2022-03-31 DOI:10.3390/dermatopathology9020015
Gehan A Pendlebury, M. Bongiorno, Jeffrey N. Lackey
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引用次数: 2

Abstract

A 19-year-old female with a history of pre-B cell acute lymphocytic leukemia (ALL) presented with two aggressive cutaneous squamous cell carcinomas (C-SCC) in the right hand. The patient was diagnosed with pre-B cell ALL at four years of age. She underwent chemotherapy with initial remission. However, recurrence of the pre-B cell ALL required an unrelated allogeneic cord hematopoietic stem cell transplant (alloHSCT). Post-transplant, the patient developed Graft-Versus-Host Disease (GVHD), which was treated with immunosuppressant therapy for six years until resolution. Fourteen years following the transplant, the patient developed a morbilliform drug eruption secondary to clindamycin. She consequently received prednisone treatment. During the treatment period, the patient developed a new ulcerated and tender nodule on the dorsal aspect of her right hand. Further histopathological biopsy confirmed the diagnosis of C-SCC, which required excision. Ten months following the excision, the patient developed an additional C-SCC nodule on the same right hand, separated by 2.6 cm from the prior C-SCC. She was referred for a ray resection procedure. This case illustrates a patient with multiple risk factors that may have contributed to the continued development of C-SCC. Such risk factors include: a prolonged course of immunosuppressant medications and voriconazole treatment. Additional research is needed to investigate the etiologies and risks of C-SCC development in patients who require a transplant and long-duration immunosuppressive therapy.
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移植物抗宿主病治疗后侵袭性皮肤鳞状细胞癌一例报告及危险因素回顾
一名有前B细胞急性淋巴细胞白血病(ALL)病史的19岁女性右手出现两例侵袭性皮肤鳞状细胞癌(C-SCC)。患者在四岁时被诊断为前B细胞ALL。她接受了化疗,病情初步缓解。然而,前B细胞ALL的复发需要进行不相关的异基因脐带造血干细胞移植(alloHSCT)。移植后,患者患上了移植物抗宿主病(GVHD),接受了六年的免疫抑制剂治疗,直到病情好转。移植14年后,患者出现了继发于克林霉素的麻疹样药疹。她因此接受了泼尼松治疗。在治疗期间,患者右手背侧出现了一个新的溃疡状、柔软的结节。进一步的组织病理学活检证实了C-SCC的诊断,需要切除。切除术后10个月,患者在同一只右手上出现了一个额外的C-SCC结节,与之前的C-SCC相距2.6厘米。她被转诊接受射线切除手术。该病例说明一名患者具有多种可能导致C-SCC持续发展的风险因素。这些风险因素包括:免疫抑制剂和伏立康唑治疗的疗程延长。需要更多的研究来调查需要移植和长期免疫抑制治疗的患者发生C-SCC的病因和风险。
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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