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以结肠髓系肉瘤为首发表现的急性早幼粒细胞白血病:1例报告并文献复习

Myeloid sarcoma of the colon as initial presentation in acute promyelocytic leukemia: A case report and review of the literature.

作者信息

Wang Lei, Cai Da-Li, Lin Na

机构信息

Department of Hematology, The First Affiliated Hospital of China Medical University, Shenyang 110001, Liaoning Province, China.

出版信息

World J Clin Cases. 2021 Jul 26;9(21):6017-6025. doi: 10.12998/wjcc.v9.i21.6017.

Abstract

BACKGROUND

Myeloid sarcoma (MS) rarely occurs in acute promyelocytic leukemia (APL) at onset, but it can develop in relapse cases, especially after APL treated with all-trans retinoic acid (ATRA). Therefore little is known about the clinical features and suitable treatment for APL related MS due to the rarity of the disease, although this may be different from the treatment and prognosis of MS in the relapse stage. To our best knowledge, this is the second case report of APL initial presentation as colon MS.

CASE SUMMARY

A 77-year-old woman complained of intermittent right lower abdominal pain, black stool, and difficult defecation for 2 mo. Physical examination showed diffuse tenderness during deep palpation and an anemic appearance. Laboratory findings showed positivity for fecal occult blood testing; white blood cell count: 3.84 × 10/L; hemoglobin: 105 g/L; platelet count: 174 × 10/L; and negativity for tumor markers. Abdominal enhanced computed tomography showed a space occupying lesion in the colon (1.9 cm). Fibrocolonoscopy revealed a polypoid and ulcerated mass measuring 2.5 cm. The tumor was removed. To our surprise, MS was confirmed by immunohistochemistry. fusion gene was detected in colon specimens by fluorescent hybridization and real-time reverse transcription polymerase chain reaction, which was consistent with the bone marrow. She was diagnosed as having APL related MS. A smooth and unobstructed intestinal wall was found by fibrocolonoscopy, and continuous molecular remission was confirmed in both the bone marrow and colon after four courses of ATRA + arsenic trioxide (ATO). ATRA + ATO showed a favorable therapeutic response for both APL and MS.

CONCLUSION

Early use of ATRA can benefit APL patients, regardless of whether MS is the first or recurrent manifestation.

摘要

背景

髓系肉瘤(MS)在急性早幼粒细胞白血病(APL)起病时很少见,但可在复发病例中发生,尤其是在接受全反式维甲酸(ATRA)治疗的APL患者中。因此,由于该疾病罕见,关于APL相关MS的临床特征和合适治疗知之甚少,尽管这可能与复发阶段MS的治疗和预后不同。据我们所知,这是第二例以结肠MS为首发表现的APL病例报告。

病例摘要

一名77岁女性主诉右下腹部间歇性疼痛、黑便及排便困难2个月。体格检查显示深触诊时有弥漫性压痛及贫血貌。实验室检查结果显示粪便潜血试验阳性;白细胞计数:3.84×10⁹/L;血红蛋白:105 g/L;血小板计数:174×10⁹/L;肿瘤标志物阴性。腹部增强计算机断层扫描显示结肠有占位性病变(1.9 cm)。纤维结肠镜检查发现一个2.5 cm的息肉样溃疡肿物。肿瘤被切除。令我们惊讶的是,免疫组化证实为MS。通过荧光原位杂交和实时逆转录聚合酶链反应在结肠标本中检测到融合基因,与骨髓一致。她被诊断为APL相关MS。纤维结肠镜检查发现肠壁光滑无梗阻,在接受四个疗程的ATRA + 三氧化二砷(ATO)治疗后,骨髓和结肠均证实持续分子缓解。ATRA + ATO对APL和MS均显示出良好的治疗反应。

结论

早期使用ATRA对APL患者有益,无论MS是首发还是复发表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f78/8316963/23a57b032f82/WJCC-9-6017-g001.jpg

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