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A rare cause of stroke in young children: minor head trauma associated with mineralising lenticulostriate angiopathy in three patients 幼儿脑卒中的一种罕见原因:三名患者的轻微头部创伤伴矿化性豆纹血管病
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-04-03 DOI: 10.1080/20469047.2022.2066386
Kiruthiga Sugumar, A. Chidambaram, B. Deepthi, S. Krishnamurthy, C. Delhikumar
ABSTRACT Acute basal ganglia infarct following minor head trauma in association with mineralisation of lenticulostriate arteries is an increasingly recognised entity in childhood stroke. Three cases with a classical history and phenotypical features of mineralising angiopathy are described. Case 1 was a 2-year-old girl who presented with acute onset hemiparesis with a same-side upper motor neuron (UMN)-type facial palsy following minor head trauma. Case 2 was a 14-month-old boy who presented with a left side hemiparesis and a left UMN-type facial nerve palsy following a minor fall. Case 3 was an 8-month-old boy who, following a fall from his cot, had a sudden-onset hemiparesis on the right side and deviation of the angle of the mouth to the left. In brain computed tomography, all three cases demonstrated characteristic basal ganglia calcification of the mineralising angiopathy. Magnetic resonance imaging of the brain demonstrated features supportive of acute infarcts in the lentiform nucleus, caudate nucleus and putamen. Two of the patients had iron deficiency anaemia with haemoglobin of 7.0 g/dL and 7.8 g/dL, respectively. On follow-up, Case 1 had mild residual weakness and the other two made a complete recovery. None of the patients had a recurrence of stroke. Basal ganglia stroke with mineralising angiopathy should be considered in toddlers presenting with sudden-onset focal neurological deficits preceded by minor head trauma. Abbreviations: ADC: apparent diffusion coefficient; CT: computed tomography; DWI: diffusion-weighted imaging; Hb: haemoglobin; IDA: iron deficiency anaemia; MRI: magnetic resonance imaging; SLV: sonographic lenticulostriate vasculopathy; SWI: susceptibility weighted imaging; UMN: upper motor neuron.
摘要轻微头部创伤后并发豆纹动脉矿化的急性基底节梗死在儿童中风中越来越被认可。描述了三例矿化血管病的经典病史和表型特征。病例1是一名2岁女孩,她在轻微头部创伤后出现急性发作性偏瘫,伴有同侧上运动神经元(UMN)型面瘫。病例2是一名14个月大的男孩,在轻微跌倒后出现左侧偏瘫和左侧UMN型面神经麻痹。病例3是一名8个月大的男孩,他从婴儿床上摔下来后,突然出现右侧偏瘫和嘴角向左偏离。在大脑计算机断层扫描中,所有三个病例都表现出矿化血管病的基底节钙化特征。大脑的磁共振成像显示了支持豆状核、尾状核和壳核急性梗死的特征。其中两名患者患有缺铁性贫血,血红蛋白分别为7.0 g/dL和7.8 g/dL。在随访中,病例1有轻微的残余虚弱,另外两例完全康复。没有一个病人中风复发。基底节卒中伴矿化血管病变的幼儿应考虑在轻微头部创伤之前出现突发性局灶性神经功能缺损。缩写:ADC:表观扩散系数;CT:计算机断层扫描;DWI:扩散加权成像;Hb:血红蛋白;IDA:缺铁性贫血;MRI:磁共振成像;SLV:超声显示的豆纹状血管病;SWI:磁化率加权成像;UMN:上运动神经元。
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引用次数: 1
A 17-year-old boy who presented with acute mononeuropathy was found to have Type 1 diabetes 一个17岁的男孩谁提出急性单神经病变被发现有1型糖尿病
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-04-03 DOI: 10.1080/20469047.2022.2059879
Fatma Özgüç Çömlek, Y. Karal, Filiz Tütüncüler
ABSTRACT Diabetic neuropathy in children and adolescents with Type 1 diabetes mellitus is rare and is usually subclinical and a complication of the late diabetes period. A 17-year-old boy admitted with a right foot drop of sudden onset was diagnosed with peroneal nerve palsy. He had had osmotic polyuria, polydipsia and weight loss for the past 2 months; his blood glucose was 25 mmol/L (<7.8), HbA1c 15.2% (4.0–5.6) and vitamin B12 125 pg/ml (180–914). The peroneal nerve palsy resolved within 3 months with blood glucose regulation and B12 supplementation. Diabetes should be borne in mind in the differential diagnosis of unusual cases of mononeuropathy. Abbreviations: DCCTS: Diabetes Control and Complications Trial Study; DM: diabetes mellitus; DN: diabetic neuropathy; GAD: glutamic acid decarboxylase; PN: peripheral neuropathy; T1DM: Type 1 diabetes mellitus.
摘要1型糖尿病儿童和青少年的糖尿病神经病变是罕见的,通常是亚临床的,是糖尿病晚期的并发症。一名17岁男孩因右脚突然下垂入院,被诊断为腓神经麻痹。在过去的两个月里,他有渗透性多尿、多饮和体重减轻;他的血糖为25 mmol/L(<7.8),HbA1c为15.2%(4.0-5.6),维生素B12为125 pg/ml(180-914)。通过血糖调节和补充B12,腓神经麻痹在3个月内得到缓解。在对不寻常的单神经病病例进行鉴别诊断时,应牢记糖尿病。缩写:DCCTS:糖尿病控制和并发症试验研究;DM:糖尿病;DN:糖尿病性神经病;GAD:谷氨酸脱羧酶;PN:周围神经病变;T1DM:1型糖尿病。
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引用次数: 3
Concomitant rapidly progressive glomerulonephritis and acute rheumatic fever after streptococcus infection: a case report 链球菌感染后并发快速进行性肾小球肾炎和急性风湿热1例
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-03-17 DOI: 10.1080/20469047.2022.2046966
Suwanna Pornrattanarungsi, S. Eursiriwan, Y. Amornchaicharoensuk, C. Chavanisakun, O. Sirimongkolchaiyakul
ABSTRACT Acute post-streptococcal glomerulonephritis (APSGN) and acute rheumatic fever (ARF) are common immune-mediated complications after group A streptococcus (GAS) infection. The causative antigenic epitopes on GAS are different for APSGN and ARF, and their simultaneous occurrence is uncommon. A 12-year-old boy presented with fever and gross haematuria. He had subcutaneous nodules on the dorsum of both feet along with a new holosystolic murmur at the apex, and he developed hypertension and generalised oedema after admission. Investigation confirmed the diagnosis of ARF with APSGN. He received a corticosteroid to control inflammation of both the conditions. His clinical signs gradually improved but he still had rheumatic heart disease. As both diseases can occur in the same patient, treatment should be provided for both conditions. Abbreviations: APSGN: acute post-streptococcal glomerulonephritis; ARF: acute rheumatic fever; ASO: antistreptolysin O; Cr: serum creatinine; CRP: C-reactive protein; ESR: erythrocyte sedimentation rate; GAS: group A streptococcus; RBC: red blood cells; RPGN: rapidly progressive glomerulonephritis; S1: first heart sound; S2: second heart sound; TTE: transthoracic echocardiogram.
摘要急性链球菌后肾小球肾炎(APSGN)和急性风湿热(ARF)是A组链球菌(GAS)感染后常见的免疫介导并发症。对于APSGN和ARF,GAS上的致病抗原表位是不同的,并且它们同时发生是罕见的。一名12岁男孩出现发烧和严重血尿。他双脚背有皮下结节,尖端有新的全收缩杂音,入院后出现高血压和全身水肿。研究证实了APSGN对ARF的诊断。他接受了皮质类固醇来控制这两种情况的炎症。他的临床症状逐渐好转,但他仍然患有风湿性心脏病。由于这两种疾病都可能发生在同一名患者身上,因此应为这两种情况提供治疗。缩写:APSGN:急性链球菌性肾小球肾炎;ARF:急性风湿热;ASO:抗链球菌溶素O;Cr:血清肌酐;CRP:C反应蛋白;ESR:红细胞沉降率;GAS:A组链球菌;RBC:红细胞;RPGN:快速进行性肾小球肾炎;S1:第一心音;S2:第二心音;TTE:经胸超声心动图。
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引用次数: 0
Trichobezoar presenting as an acute abdominal obstruction in a 17-year-old girl 毛牛黄表现为一名17岁女孩的急性腹部梗阻
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-03-06 DOI: 10.1080/20469047.2022.2045691
Z. Bayramoğlu, R. Comert, B. Erginel, Abdulkadir Baziki
ABSTRACT Trichobezoars are hairballs that combine with food residue in the digestive tract as a result of ingesting hair. A 17-year-old girl was admitted to the emergency department with abdominal pain and vomiting for 3 days. She had been having digestive difficulty and bloating for the previous 2 months. An abdominal radiograph demonstrated air-fluid levels consistent with ileus, and an ultrasound showed hyperechoic material in the stomach and ileum. Computed tomography demonstrated images of trapped air which was considered diagnostic of a bezoar. At laparotomy, a large mass was removed from the stomach. As the bezoar extended through the pylorus and duodenum and there were mobile masses palpable in the ileum, it required a second incision to remove them. For some years she had had a habit of swallowing hair which she found on her pillow and there was a history of an obsessive personality trait and hyperactivity for which she agreed to attend a psychiatric clinic. Abbreviations: BMI: body mass index; CT: computed tomography; Hb: haemoglobin; IV: intravenous; WHO: World Health Organization
摘要毛霉菌是一种毛球,由于摄入毛发而在消化道中与食物残渣结合。一名17岁女孩因腹痛和呕吐入院3天。在过去的两个月里,她一直有消化困难和腹胀。腹部X光片显示空气液体水平与回肠一致,超声波显示胃和回肠中有高回声物质。计算机断层扫描显示了被困空气的图像,这被认为是牛黄的诊断。在剖腹手术中,从胃中取出了一个大肿块。由于牛黄延伸穿过幽门和十二指肠,回肠中有可触及的活动肿块,因此需要第二次切开将其切除。几年来,她一直有吞咽枕头上发现的头发的习惯,而且有强迫症和多动症的病史,为此她同意去精神科诊所。缩写:BMI:体重指数;CT:计算机断层扫描;Hb:血红蛋白;IV: 静脉注射;世界卫生组织:世界卫生组织
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引用次数: 0
Splenic rupture presenting with marked scrotal ecchymosis in a 2-day-old newborn. 脾破裂表现为明显的阴囊淤血在一个2天大的新生儿。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2021-09-13 DOI: 10.1080/20469047.2021.1971923
Gaffari Tunc, Cengiz Güney, Utku Aygüneş

Splenic rupture is a rare and severe condition in neonates. The signs and symptoms are vague and non-specific and are often not recognised before the onset of hypovolaemic shock or death. A 2-day-old infant presented with scrotal ecchymosis, and ultrasonography detected haemorrhage in the scrotal, right inguinal and adrenal regions. Computed tomography demonstrated a peri-splenic haematoma. Haemoglobin (Hb) was 2.79 g/dL and, despite repeated transfusions, the Hb level could not be sustained. Exploratory laparotomy detected a large haematoma in the splenic region, and, because of the uncontrolled haemorrhage, splenectomy was required.

脾破裂是一种罕见且严重的新生儿疾病。体征和症状模糊且无特异性,在低血容量性休克或死亡发生前往往无法识别。一个2天大的婴儿表现为阴囊淤斑,超声检查发现阴囊、右腹股沟和肾上腺区出血。计算机断层显示脾周血肿。血红蛋白(Hb)为2.79 g/dL,尽管多次输血,Hb水平仍无法维持。剖腹探查发现脾区有一个大血肿,由于出血无法控制,需要脾切除术。
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引用次数: 0
Acute demyelination of the medulla oblongata owing to scrub typhus in a 7-year-old boy: case report. 7岁男童因恙虫病致延髓急性脱髓鞘:个案报告。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2022-02-08 DOI: 10.1080/20469047.2022.2035622
Srinanda Majumder, Moumita Samanta, Tapan Kumar Sinha Mahapatra

Abbreviations: ADEM: acute disseminated encephalomyelitis; CT: computed tomography; MRI: magnetic resonance imaging; PGCS: paediatric Glasgow coma scale; PICU: paediatric intensive care unit.

ADEM:急性播散性脑脊髓炎;CT:计算机断层扫描;MRI:磁共振成像;PGCS:儿童格拉斯哥昏迷量表;PICU:儿科重症监护病房。
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引用次数: 0
Neonatal palliative care practices: an Indian perspective. 新生儿姑息治疗实践:印度的观点。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2022-06-21 DOI: 10.1080/20469047.2022.2089821
Dwayne Mascarenhas, Medha Goyal, Ruchi Nanavati

Background: Neonatal palliative care (NPC) aims to prevent and relieve the suffering of neonates who are not going to recover. Although an integral part of neonatal care, it remains in nascent stages in many parts of the world.

Aim: To describe neonatologists' level of knowledge and understanding of NPC, and to describe current practices and barriers to its delivery.

Methods: The study, a cross-sectional web-based national survey, was undertaken between 2019 and 2020. A structured form of 22 questions about NPC was completed by neonatologists across level III neonatal intensive care units in India.

Results: Of the 145 questionnaires sent out, 65 responses were returned (44.8%). The participating units were in both public (38.5%) and private/corporate hospitals (61.5%). The concept of NPC was known to 90.8%, and 93.8% could identify conditions necessitating palliation. However, 81.5% of units lacked a palliative team, and few had teams of only neonatologists and neonatal nurses. Only 10.8% of the units had a structured policy, but none addressed all aspects of neonatal palliation. The creation of memories by parents spending time with their neonate (38.9%), photography (75.9%), footprints (13%) or collecting memorabilia was allowed at many centres. Frequently encountered barriers included inadequate knowledge (16.9%), poor infrastructure (21.5%), inadequate human resources (24.6%) and a lack of structured guidelines and legal support (15.4%).

Conclusion: This is the first study to highlight a large gap in neonatal end-of-life care in India and it reflects an urgent need to facilitate its incorporation into routine care.

Abbreviations: NICU: neonatal intensive care unit; NPC: neonatal palliative care.

背景:新生儿姑息治疗(NPC)的目的是预防和减轻新生儿的痛苦谁是不会恢复。虽然它是新生儿护理的一个组成部分,但在世界许多地方仍处于初级阶段。目的:描述新生儿医生对鼻咽癌的知识和理解水平,并描述目前的做法和障碍。方法:该研究是一项基于网络的横断面全国调查,于2019年至2020年进行。印度三级新生儿重症监护病房的新生儿专家完成了一份包含22个NPC问题的结构化表格。结果:共发放问卷145份,回收65份,回收率为44.8%。参与调查的单位既有公立医院(38.5%),也有私立/企业医院(61.5%)。90.8%的人知道NPC的概念,93.8%的人能识别需要姑息治疗的病情。然而,81.5%的单位缺乏姑息治疗团队,很少有只有新生儿医生和新生儿护士的团队。只有10.8%的单位有结构化的政策,但没有一个涉及新生儿姑息治疗的所有方面。许多中心允许父母与新生儿共度时光(38.9%)、拍照(75.9%)、留下脚印(13%)或收集纪念品来创造记忆。经常遇到的障碍包括知识不足(16.9%)、基础设施差(21.5%)、人力资源不足(24.6%)以及缺乏结构化指导方针和法律支持(15.4%)。结论:这是第一项研究,突出了印度新生儿临终关怀的巨大差距,它反映了迫切需要促进其纳入日常护理。缩写:NICU:新生儿重症监护病房;新生儿姑息治疗。
{"title":"Neonatal palliative care practices: an Indian perspective.","authors":"Dwayne Mascarenhas,&nbsp;Medha Goyal,&nbsp;Ruchi Nanavati","doi":"10.1080/20469047.2022.2089821","DOIUrl":"https://doi.org/10.1080/20469047.2022.2089821","url":null,"abstract":"<p><strong>Background: </strong>Neonatal palliative care (NPC) aims to prevent and relieve the suffering of neonates who are not going to recover. Although an integral part of neonatal care, it remains in nascent stages in many parts of the world.</p><p><strong>Aim: </strong>To describe neonatologists' level of knowledge and understanding of NPC, and to describe current practices and barriers to its delivery.</p><p><strong>Methods: </strong>The study, a cross-sectional web-based national survey, was undertaken between 2019 and 2020. A structured form of 22 questions about NPC was completed by neonatologists across level III neonatal intensive care units in India.</p><p><strong>Results: </strong>Of the 145 questionnaires sent out, 65 responses were returned (44.8%). The participating units were in both public (38.5%) and private/corporate hospitals (61.5%). The concept of NPC was known to 90.8%, and 93.8% could identify conditions necessitating palliation. However, 81.5% of units lacked a palliative team, and few had teams of only neonatologists and neonatal nurses. Only 10.8% of the units had a structured policy, but none addressed all aspects of neonatal palliation. The creation of memories by parents spending time with their neonate (38.9%), photography (75.9%), footprints (13%) or collecting memorabilia was allowed at many centres. Frequently encountered barriers included inadequate knowledge (16.9%), poor infrastructure (21.5%), inadequate human resources (24.6%) and a lack of structured guidelines and legal support (15.4%).</p><p><strong>Conclusion: </strong>This is the first study to highlight a large gap in neonatal end-of-life care in India and it reflects an urgent need to facilitate its incorporation into routine care.</p><p><strong>Abbreviations: </strong>NICU: neonatal intensive care unit; NPC: neonatal palliative care.</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2022-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40163452","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Co-existing sickle cell anaemia and inflammatory bowel disease: case report and review of the literature. 并存的镰状细胞性贫血和炎症性肠病:病例报告和文献回顾。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2021-09-03 DOI: 10.1080/20469047.2021.1936393
A A Adepoju, A Akere, G O Ogun, B O Ogunbosi, A O Asinobi, O Bello, A E Orimadegun, S Allen, O O Akinyinka

Sickle cell anaemia (SCA) is a chronic haemolytic anaemia associated with vaso-occlusive painful crises which may affect several systems including the gastro-intestinal system, resulting in abdominal pain. The concurrence of inflammatory bowel disease and haemoglobinopathy is rare. No previously reported concurrent cases of both SCA and ulcerative colitis (UC) in sub-Saharan Africa were found in the literature. A 16-year-old girl with concurrent SCA and UC is presented. She was admitted to University College Hospital, Ibadan with a 1-year history of recurrent peri-umbilical pain and bloody stools. These symptoms were mainly attributed to SCA at the referring hospital, and she was managed for chronic tropical diarrhoea without a remarkable clinical response. This case illustrates the concurrent presentation of SCA and ulcerative colitis which led to the missed and delayed diagnosis of ulcerative colitis.

镰状细胞性贫血(SCA)是一种慢性溶血性贫血,与血管闭塞性疼痛危机相关,可影响包括胃肠道系统在内的多个系统,导致腹痛。炎症性肠病和血红蛋白病同时发生是罕见的。文献中未发现撒哈拉以南非洲地区SCA和溃疡性结肠炎(UC)同时发生的病例。一个16岁的女孩同时患有SCA和UC。她因复发性脐周疼痛和便血病史1年而入住伊巴丹大学学院医院。这些症状主要归因于转诊医院的SCA,她被治疗为慢性热带腹泻,但没有显著的临床反应。本病例说明SCA和溃疡性结肠炎同时出现,导致溃疡性结肠炎的漏诊和延迟诊断。
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引用次数: 2
Iron-deficiency anaemia in childhood: a risk factor for severe venous thrombosis? 儿童缺铁性贫血:严重静脉血栓形成的危险因素?
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2021-05-18 DOI: 10.1080/20469047.2021.1923301
Antonietta Curatola, Serena Ferretti, Antonio Gatto, Piero Valentini, Ilaria Lazzareschi

Iron deficiency anaemia is a common disorder in the paediatric age-group. The association between iron deficiency and venous thrombosis in children without an underlying illness is rare. Two cases are described. A 17-year-old girl had been taking oestrogen-progestogen therapy for contraception for about 2 years and developed a lower-limb deep vein thrombosis associated with pulmonary embolism. A 3-year-old girl was admitted to the paediatric emergency department with pallor, weakness and vomiting, and a cerebral CT showed a recent cerebral venous thrombosis. Both cases had severe iron-deficiency anaemia which increases a thrombotic tendency and could be a further crucial trigger of venous thrombosis in patients at low risk; therefore, in cases of unexplained thrombosis, it must always be considered to be a risk factor.Abbreviations APCR: activated protein C resistance; CMV: cytomegalovirus; CT: computerised tomography; CVST: cerebral venous sinus thrombosis; CVT: cerebral venous thrombosis; DVT: deep vein thrombosis; DOACs: direct oral anticoagulants; EBV: Epstein-Barr virus; ID: iron deficiency; IDA: iron deficiency anaemia; LMWH: low molecular weight heparin; PE: pulmonary embolism; RDW: red blood cell distribution width; VT: venous thrombosis.

缺铁性贫血是一种常见的疾病在儿科年龄组。在没有基础疾病的儿童中,缺铁和静脉血栓形成之间的联系是罕见的。本文描述了两个案例。一个17岁的女孩服用雌激素-孕激素治疗避孕约2年,并发下肢深静脉血栓并肺栓塞。一名3岁女孩因面色苍白、虚弱和呕吐被送入儿科急诊科,脑CT显示近期脑静脉血栓形成。这两个病例都有严重的缺铁性贫血,这增加了血栓形成的倾向,可能是低风险患者静脉血栓形成的进一步关键触发因素;因此,在不明原因血栓形成的情况下,必须始终将其视为一个危险因素。APCR:活化蛋白C抗性;巨细胞病毒:巨细胞病毒;CT:计算机断层扫描;CVST:脑静脉窦血栓形成;CVT:脑静脉血栓形成;DVT:深静脉血栓;DOACs:直接口服抗凝剂;eb: eb病毒;ID:缺铁;IDA:缺铁性贫血;LMWH:低分子肝素;PE:肺栓塞;RDW:红细胞分布宽度;VT:静脉血栓。
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引用次数: 2
A gastric outlet thickened mucosal fold associated with cytomegalovirus infection in an extremely preterm infant managed by surgical resection. 手术切除一例极早产儿胃出口粘膜增厚伴巨细胞病毒感染。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2022-02-01 Epub Date: 2021-09-14 DOI: 10.1080/20469047.2021.1967626
Susmitha Tangirala, Prakash Amboiram, Umamaheswari Balakrishnan, Sandhya Sundaram, Prakash Agarwal, Usha Devi

Non-bilious vomiting in preterm neonates discharged from neonatal intensive care units is a common complaint and is often associated with benign conditions such as gastro-oesophageal reflux. A neonate of 27 weeks gestation who presented later with vomiting owing to gastric outlet obstruction is described. He was discharged at 11 weeks of age and required re-admission 1 week later. He had persistent non-bilious vomiting from 7 weeks of age, failure to thrive and metabolic alkalosis. Clinical examination demonstrated visible gastric peristalsis, and hypertrophic pyloric stenosis was suspected. Ultrasound of the gastric pylorus and upper gastro-intestinal contrast studies were negative. Exploratory laparotomy after failure of conservative management revealed a thickened mucosal fold in the gastric pylorus, which was excised. Histopathology demonstrated inclusion bodies which are pathognomonic of cytomegalovirus infection. He was treated with valganciclovir for 6 weeks and was asymptomatic and thriving well at follow-up. Gastric outlet obstruction can be one of the manifestations of CMV infection of the gastro-intestinal tract. Diagnosis can be confirmed only by histopathology.Abbreviations: BPD: bronchopulmonary dysplasia; CMV: cytomegalovirus; H&E: haematoxylin and eosin; IHC: immunohistochemistry; IHPS: infantile hypertrophic pyloric stenosis; NEC: necrotising enterocolitis; PCR: polymerase-chain reaction; VGP: visible gastric peristalsis.

从新生儿重症监护病房出院的早产儿非胆汁性呕吐是一种常见的主诉,通常与胃食管反流等良性疾病有关。一个27周妊娠的新生儿谁提出后来呕吐由于胃出口梗阻的描述。11周龄出院,1周后再次入院。他从7周龄开始出现持续的非胆汁性呕吐,发育不良和代谢性碱中毒。临床检查可见胃蠕动,怀疑幽门肥厚性狭窄。胃幽门超声及上消化道造影均为阴性。保守治疗失败后剖腹探查发现幽门黏膜增厚,并切除。组织病理学证实包涵体是巨细胞病毒感染的典型特征。患者经缬更昔洛韦治疗6周,无症状,随访情况良好。胃出口梗阻是巨细胞病毒感染胃肠道的表现之一。诊断只能通过组织病理学证实。缩写:BPD:支气管肺发育不良;巨细胞病毒:巨细胞病毒;H&E:血红素和伊红;包含IHC:免疫组织化学;IHPS:婴儿肥厚性幽门狭窄;NEC:坏死性小肠结肠炎;PCR:聚合酶链反应;VGP:可见胃蠕动。
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引用次数: 1
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Paediatrics and International Child Health
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