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儿童膀胱粒细胞肉瘤:病例报告及文献综述

Bladder granulocytic sarcoma in a child: case report and literature review.

作者信息

Tuna Rumeysa, Karaman Serap, Oktar Tayfun, Anak Sema, Doğan Öner, Ünüvar Ayşegül, Tuğcu Deniz, Bayramoğlu Zuhal, Kılıç Suar Çakı, Çelik Ayça İribaş, Karakaş Zeynep

机构信息

Departments of Pediatric Hematology and Oncology, İstanbul University Faculty of Medicine, İstanbul, Turkey.

Departments of Urology, İstanbul University Faculty of Medicine, İstanbul, Turkey.

出版信息

Turk J Pediatr. 2022;64(1):152-159. doi: 10.24953/turkjped.2020.275.

Abstract

BACKGROUND

Granulocytic sarcoma (GS) is an extramedullary solid tumor composed of immature myeloid cells. GS has been associated with acute myeloid leukemia (AML), myelodysplastic syndromes or myeloproliferative diseases. Although GS can affect various tissues of the human body, it has rarely been reported in other soft tissues such as the breast, gastrointestinal, respiratory and genitourinary tracts. We report a pediatric case diagnosed with granulocytic sarcoma of the bladder and concomitant AML.

CASE

A twelve-year-old previously healthy girl was admitted to the pediatric urology clinic with a ten-day history of hematuria and pollakiuria. Laboratory examinations revealed anemia, thrombocytopenia and neutrophilic leukocytosis. Bone marrow aspiration results were consistent with acute myeloid leukemia -FAB subtype M2-. Abdominal magnetic resonance imaging (MRI) showed an irregularly bounded 12 cm mass on the right side of the bladder. Transurethral resection (TUR) pathology was consistent with granulocytic sarcoma. After a multimodal treatment approach, complete remission was achieved.

CONCLUSIONS

Malignant bladder masses are rare causes of macroscopic hematuria in childhood. The diagnostic spectrum is wide, ranging from rhabdomyosarcoma to leukemia involvement. The bladder is a rare site of extramedullary involvement in pediatric patients with AML. Multimodal treatment should be considered on a per-patient basis.

摘要

背景

粒细胞肉瘤(GS)是一种由未成熟髓样细胞组成的髓外实体瘤。GS与急性髓系白血病(AML)、骨髓增生异常综合征或骨髓增殖性疾病有关。尽管GS可累及人体的各种组织,但在乳腺、胃肠道、呼吸道和泌尿生殖道等其他软组织中鲜有报道。我们报告一例诊断为膀胱粒细胞肉瘤并伴有AML的儿科病例。

病例

一名12岁既往健康的女孩因血尿和尿频10天入住儿科泌尿外科诊所。实验室检查显示贫血、血小板减少和中性粒细胞增多。骨髓穿刺结果与急性髓系白血病-FAB亚型M2-相符。腹部磁共振成像(MRI)显示膀胱右侧有一个边界不规则的12cm肿块。经尿道切除术(TUR)病理结果与粒细胞肉瘤相符。经过多模式治疗,实现了完全缓解。

结论

恶性膀胱肿块是儿童肉眼血尿的罕见原因。诊断范围广泛,从横纹肌肉瘤到白血病累及。膀胱是小儿AML患者髓外累及的罕见部位。应根据患者个体情况考虑多模式治疗。

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