Sarkar Sayan, Ghosh Priya, Gehani Anisha, Ghara Niharendu, Bhattacharyya Parthasarathi
Department of Radiology, Tata Medical Center, 14 MAR (E-W), New Town, Rajarhat, Kolkata, 700160, West Bengal, India.
Department of Pediatric Haematology, Tata Medical Center, 14 MAR (E-W), New Town, Rajarhat, Kolkata, 700160, West Bengal, India.
J Med Case Rep. 2021 May 5;15(1):226. doi: 10.1186/s13256-021-02790-w.
Differentiation syndrome (DS) is a life-threatening complication that may be seen in patients with acute promyelocytic leukaemia undergoing induction therapy with all-trans retinoic acid or arsenic trioxide. It can lead to severe inflammatory response syndrome and shock if adequate measures are not taken immediately. The radiological features of lung nodules with changes in ground-glass opacity can represent DS. The principal unique feature of the case reported here is that the diagnosis of DS was based on imaging results in the absence of a low total leukocyte count.
A 14-year-old Indian girl diagnosed with acute promyelocytic leukaemia currently undergoing a chemotherapy regimen that included all-trans retinoic acid/arsenic trioxide was sent to the radiology department for investigation of respiratory distress which she had developed soon after the initiation of chemotherapy. Her chest radiograph showed bilateral lower zone lung infiltrates. Computed tomography (CT) revealed changes in ground-glass opacity in the lower lobes with multiple lung nodules. Differential diagnosis included bacterial, viral or fungal infections, leukemic infiltrates, drug toxicity, pulmonary haemorrhage or leukostasis. She was started on dexamethasone immediately after stopping the chemotherapy with all-trans retinoic acid/arsenic trioxide and given ventilatory support. Her condition subsequently improved and her follow-up chest radiograph and CT scan showed a significant reduction of abnormal lung findings. Based on the clinical improvement and the resolution of findings on imaging following the withdrawal of all-trans retinoic acid/arsenic trioxide, we made the diagnosis of DS.
Though a rather unusual possibility, the treatment history of the patient enabled a rather crucial diagnosis in the nick of time and imaging played a pivotal role. This case further iterates the importance of keeping DS in mind when dealing with similar patients in the future.
分化综合征(DS)是一种危及生命的并发症,见于接受全反式维甲酸或三氧化二砷诱导治疗的急性早幼粒细胞白血病患者。若不立即采取适当措施,可导致严重炎症反应综合征和休克。伴有磨玻璃影改变的肺结节的影像学特征可提示DS。本文报道病例的主要独特之处在于,DS的诊断基于影像学结果,而此时患者白细胞总数并未降低。
一名14岁印度女孩被诊断为急性早幼粒细胞白血病,目前正在接受包含全反式维甲酸/三氧化二砷的化疗方案,化疗开始后不久出现呼吸窘迫,遂被送往放射科检查。她的胸部X光片显示双侧下肺野浸润。计算机断层扫描(CT)显示下叶磨玻璃影改变伴多发肺结节。鉴别诊断包括细菌、病毒或真菌感染、白血病浸润、药物毒性、肺出血或白细胞淤滞。停用全反式维甲酸/三氧化二砷化疗后,立即给予她地塞米松并进行通气支持。她的病情随后好转,随访胸部X光片和CT扫描显示肺部异常表现显著减轻。基于临床症状改善以及停用全反式维甲酸/三氧化二砷后影像学检查结果的消退,我们做出了DS的诊断。
尽管可能性不大,但患者的治疗史及时促成了关键诊断,影像学发挥了关键作用。该病例进一步强调了未来在处理类似患者时牢记DS的重要性。