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一名20个月大患有横纹肌肉瘤的女婴右脚毛细血管再充盈时间显著延长。

Marked Prolongation of Capillary Refill Time in the Right Foot of a 20-Month-Old Female Infant With Rhabdomyosarcoma.

作者信息

Fukushima Hiroko, Kawahara Sakura, Yamaki Yuni

机构信息

Department of Child Health, University of Tsukuba, Tsukuba, JPN.

Department of Pediatrics, University of Tsukuba Hospital, Tsukuba, JPN.

出版信息

Cureus. 2025 Aug 27;17(8):e91142. doi: 10.7759/cureus.91142. eCollection 2025 Aug.

Abstract

Childhood cancer is a rare condition. Motor dysfunction may be an initial manifestation of a solid tumor, particularly when caused by spinal or vascular compression. However, in infants who have only recently begun to walk, such symptoms may be misinterpreted as normal developmental variations. Additionally, vascular signs such as delayed capillary refill time (CRT) are extremely rare and may easily be overlooked in clinical practice. Prompt diagnosis and intervention are essential to preserve neurological function in cases of spinal cord compression. Nevertheless, due to the rarity of such presentations, primary care providers, including pediatricians, may have limited experience. A 20-month-old girl presented with right lower limb weakness, bladder and bowel dysfunction, and fever. She had begun walking at 12 months but developed a limp at 18 months. One month prior to admission, she exhibited sensory deficits and diminished reflexes in the right leg, which were initially attributed to her history of prematurity at birth. At 20 months of age, she stopped using her right leg entirely and was admitted to our hospital. Physical examination revealed decreased muscle strength of the right lower limb (knee and ankle joints, manual muscle test grade 4), coldness and prolonged CRT in the right foot, and right thigh swelling (right 26 cm; left 23.5 cm). Computed tomography revealed a large pelvic mass compressing the vasculature and spinal cord, along with another mass from T7 to T9. Multimodal chemotherapy was initiated immediately prior to establishing a final diagnosis. Capillary refill improved within one week, and the thigh asymmetry resolved by day 11. The final histological diagnosis confirmed stage 4 embryonal rhabdomyosarcoma. A very good partial response was achieved after 12 months of treatment. She regained partial ambulation using a brace; however, bladder and bowel dysfunction persisted. This case highlights the diagnostic challenges in identifying malignancy in young children presenting with subtle neurological or vascular symptoms. Previous reports on impaired blood flow in the lower extremities among pediatric cancer patients, including those with rhabdomyosarcoma, have been limited. Although rarely reported in the literature, such presentations are occasionally encountered in daily clinical practice. Previous studies have shown that delayed diagnosis of spinal cord compression is associated with poorer neurological outcomes, particularly in younger patients. Earlier recognition of asymmetry and impaired perfusion in the lower limbs might have enabled more timely diagnosis and intervention in this case.

摘要

儿童癌症是一种罕见疾病。运动功能障碍可能是实体瘤的初始表现,尤其是由脊髓或血管受压引起时。然而,在刚学会走路的婴儿中,此类症状可能会被误解为正常的发育变异。此外,诸如毛细血管再充盈时间(CRT)延迟等血管体征极为罕见,在临床实践中很容易被忽视。对于脊髓受压病例,及时诊断和干预对于保留神经功能至关重要。然而,由于此类表现罕见,包括儿科医生在内的基层医疗服务提供者可能经验有限。一名20个月大的女孩出现右下肢无力、膀胱和肠道功能障碍以及发热。她12个月开始走路,但18个月时出现跛行。入院前一个月,她右腿出现感觉减退和反射减弱,最初归因于早产史。20个月大时,她完全不再使用右腿,并入住我院。体格检查发现右下肢肌力下降(膝关节和踝关节,徒手肌力测试4级),右脚发凉且CRT延长,右大腿肿胀(右侧26厘米;左侧23.5厘米)。计算机断层扫描显示一个巨大的盆腔肿块压迫血管和脊髓,同时还有一个从T7到T9的肿块。在最终确诊前立即开始多模式化疗。一周内毛细血管再充盈情况改善,第11天时大腿不对称情况得到缓解。最终组织学诊断证实为4期胚胎性横纹肌肉瘤。治疗12个月后取得了非常好的部分缓解。她使用支具恢复了部分行走能力;然而,膀胱和肠道功能障碍仍然存在。该病例突出了在识别出现细微神经或血管症状的幼儿恶性肿瘤时的诊断挑战。先前关于儿科癌症患者(包括横纹肌肉瘤患者)下肢血流受损的报道有限。尽管文献中很少报道,但此类表现在日常临床实践中偶尔会遇到。先前的研究表明,脊髓受压的延迟诊断与较差的神经学预后相关,尤其是在较年轻的患者中。更早识别下肢的不对称和灌注受损可能会使该病例得到更及时的诊断和干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c49/12476274/5411891c1968/cureus-0017-00000091142-i01.jpg

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