Approach to a Child with Bilateral Proptosis as a Rare Presentation of Acute Myeloid Leukemia

Shafiq Tanveer, Maryum Khilji, Rao Hassan, Safina Tanveer, Ayesha Khilji
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 Categories: Ophthalmology, Pediatrics, Hematology","PeriodicalId":7672,"journal":{"name":"American Journal of Health, Medicine and Nursing Practice","volume":"233 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Health, Medicine and Nursing Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47672/ajhmn.1600","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

A 6-year-old girl presented with a 2-month history of sudden onset, painless, progressively increasing bilateral proptosis, palpable lymphadenopathy and skin pallor. A full blood count showed bicytopenia and the erythrocyte sedimentation rate (ESR) was raised. Computerized tomography (CT) scan showed bilateral lacrimal gland enlargement. The bone marrow biopsy was consistent with M2 acute myeloid leukemia (AML). The patient received symptomatic treatment and was sent to pediatric oncologist for induction chemotherapy and tumor lysis syndrome (TLS) protocol. Bilateral proptosis is a rare manifestation of several diseases. This case report emphasizes on the low threshold for hematological malignancies in the presentation of bilateral proptosis. Ophthalmologists should be cognizant of the unusual ophthalmic manifestations of haematological malignancies, as they are a diagnostic challenge but knowledge about the rare extramedullary manifestations of AML facilitates early diagnosis and thereby improves prognosis. Categories: Ophthalmology, Pediatrics, Hematology
一例罕见的急性髓系白血病患儿双侧突出的治疗方法
一名6岁女孩,表现为2个月的突然发病,无痛,渐进性双侧突出,可触及的淋巴结病和皮肤苍白。全血细胞计数显示双氧体减少和红细胞沉降率(ESR)升高。CT扫描显示双侧泪腺肿大。骨髓活检符合M2型急性髓性白血病(AML)。对症治疗后送儿科肿瘤科进行诱导化疗及肿瘤溶解综合征(TLS)治疗方案。双侧突出是几种疾病的罕见表现。本病例报告强调双侧突出表现为血液系统恶性肿瘤的低阈值。眼科医生应该认识到血液系统恶性肿瘤的不寻常的眼部表现,因为它们是一个诊断挑战,但了解AML罕见的髓外表现有助于早期诊断,从而改善预后。 分类:眼科,儿科,血液学
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