keratoacanthomas are common
角化棘皮瘤很常见
multiple keratoacanthomas
多发性角化棘皮瘤
treating keratoacanthomas
治疗角化棘皮瘤
diagnosing keratoacanthomas
诊断角化棘皮瘤
keratoacanthomas developing
角化棘皮瘤发展
keratoacanthomas appearing
角化棘皮瘤出现
keratoacanthomas regressing
角化棘皮瘤消退
keratoacanthomas confirmed
确诊角化棘皮瘤
keratoacanthomas removed
切除角化棘皮瘤
keratoacanthomas excised
切除角化棘皮瘤
multiple keratoacanthomas appeared on the patient's arms and face following sun exposure.
患者的胳膊和脸上出现多个角化棘瘤，继发于阳光照射后。
the dermatologist performed a biopsy to confirm the diagnosis of keratoacanthomas versus squamous cell carcinoma.
皮肤科医生进行了活检以确认角化棘瘤与鳞状细胞癌的诊断。
eruptive keratoacanthomas are a rare variant that requires specialized treatment approaches.
爆发性角化棘瘤是一种罕见的变异，需要专门的治疗方法。
keratoacanthomas typically regress spontaneously within six months without treatment.
角化棘瘤通常在六个月内自发消退，无需治疗。
the surgical excision of keratoacanthomas provides the most definitive treatment option.
手术切除是治疗角化棘瘤最具确定性的治疗选择。
ferguson-smith syndrome is characterized by multiple familial keratoacanthomas.
费金森-史密斯综合征的特征是多发性家族性角化棘瘤。
topical methotrexate has shown efficacy in treating keratoacanthomas in some patients.
局部使用甲氨蝶呤已被证明对某些患者的角化棘瘤有效。
the rapid growth phase of keratoacanthomas often alarms patients who seek immediate medical attention.
角化棘瘤的快速生长阶段常常让寻求立即医疗关注的患者感到担忧。
histopathological examination remains the gold standard for diagnosing keratoacanthomas accurately.
组织病理学检查仍然是准确诊断角化棘瘤的金标准。
some researchers classify keratoacanthomas as well-differentiated variants of squamous cell carcinoma.
一些研究人员将角化棘瘤归类为分化良好的鳞状细胞癌变异。
the patient reported that the keratoacanthoma lesion became painful and pruritic before spontaneous regression.
患者报告称，在角化棘瘤病变自发消退之前，变得疼痛和瘙痒。
immunosuppressed individuals have a higher risk of developing aggressive keratoacanthomas.
免疫抑制个体患侵袭性角化棘瘤的风险更高。
keratoacanthomas are common
角化棘皮瘤很常见
multiple keratoacanthomas
多发性角化棘皮瘤
treating keratoacanthomas
治疗角化棘皮瘤
diagnosing keratoacanthomas
诊断角化棘皮瘤
keratoacanthomas developing
角化棘皮瘤发展
keratoacanthomas appearing
角化棘皮瘤出现
keratoacanthomas regressing
角化棘皮瘤消退
keratoacanthomas confirmed
确诊角化棘皮瘤
keratoacanthomas removed
切除角化棘皮瘤
keratoacanthomas excised
切除角化棘皮瘤
multiple keratoacanthomas appeared on the patient's arms and face following sun exposure.
患者的胳膊和脸上出现多个角化棘瘤，继发于阳光照射后。
the dermatologist performed a biopsy to confirm the diagnosis of keratoacanthomas versus squamous cell carcinoma.
皮肤科医生进行了活检以确认角化棘瘤与鳞状细胞癌的诊断。
eruptive keratoacanthomas are a rare variant that requires specialized treatment approaches.
爆发性角化棘瘤是一种罕见的变异，需要专门的治疗方法。
keratoacanthomas typically regress spontaneously within six months without treatment.
角化棘瘤通常在六个月内自发消退，无需治疗。
the surgical excision of keratoacanthomas provides the most definitive treatment option.
手术切除是治疗角化棘瘤最具确定性的治疗选择。
ferguson-smith syndrome is characterized by multiple familial keratoacanthomas.
费金森-史密斯综合征的特征是多发性家族性角化棘瘤。
topical methotrexate has shown efficacy in treating keratoacanthomas in some patients.
局部使用甲氨蝶呤已被证明对某些患者的角化棘瘤有效。
the rapid growth phase of keratoacanthomas often alarms patients who seek immediate medical attention.
角化棘瘤的快速生长阶段常常让寻求立即医疗关注的患者感到担忧。
histopathological examination remains the gold standard for diagnosing keratoacanthomas accurately.
组织病理学检查仍然是准确诊断角化棘瘤的金标准。
some researchers classify keratoacanthomas as well-differentiated variants of squamous cell carcinoma.
一些研究人员将角化棘瘤归类为分化良好的鳞状细胞癌变异。
the patient reported that the keratoacanthoma lesion became painful and pruritic before spontaneous regression.
患者报告称，在角化棘瘤病变自发消退之前，变得疼痛和瘙痒。
immunosuppressed individuals have a higher risk of developing aggressive keratoacanthomas.
免疫抑制个体患侵袭性角化棘瘤的风险更高。
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