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High-output Cervical Chylous Fistula in a Child: Successful Conservative Management. 1例儿童高输出颈乳糜瘘:成功的保守治疗。
Q3 Medicine Pub Date : 2025-09-01 DOI: 10.4103/jiaps.jiaps_126_25
Nikolaos Baltogiannis
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引用次数: 0
Dorsal Tilt of Penis with Orthotopic Urethral Meatus in a 6-year-old Child. 1例6岁儿童阴茎后倾伴尿道道原位。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-05-21 DOI: 10.4103/jiaps.jiaps_38_25
Rohit Lal, Md Zeeshan Anwar, Vinit Kumar Thakur

The penis should ideally be straight. Chordee is most commonly associated with hypospadias and epispadias; ventral chordee with hypospadias and dorsal chordee with epispadias, although they can also be seen in orthotopic meatus. One reason for a dorsal curvature of the penis might be improper saddling of the fundiform ligament on the dorsal shaft of the penis. The study documented the surgical treatment of a 6-year-old boy with isolated dorsal tilt of the penis.

阴茎最好是直的。脊索最常与尿道下裂和尿道上裂有关;腹侧脊索伴尿道下裂,背侧脊索伴尿道上裂,尽管它们也可以在正位食管中看到。阴茎背弯的一个原因可能是阴茎背轴上的底状韧带鞍位不当。本研究记录了一例6岁男童孤立性阴茎背倾斜的手术治疗。
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引用次数: 0
Accessory Liver Lobe in Hernia of Umbilical Cord with Radial Limb Anomaly in a Neonate: A Rare Association. 新生儿脐带疝伴桡肢异常的副肝:罕见的关联。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-05-05 DOI: 10.4103/jiaps.jiaps_42_25
Vijay Kumar Kundal, Gali Divya, Akshat Sudhanshu, Pinaki Ranjan Debnath

The author reports a rare case of umbilical cord hernia with the accessory lobe of the liver entrapped in the amniotic sac with radial limb anomaly with malrotation. The accessory lobe of the liver is a rare anatomical variant of the liver that is often asymptomatic. The accessory lobe of the liver causing nonclosure of the umbilical ring is also very rare. The accessory lobe of the liver was formed during the development of embryonic body wall folds and disturbed the complete closure of the umbilical ring. If a clear-cut diagnosis of the accessory lobe is made, then it should be resected. In case of doubt, it should be fixed to the abdominal wall and regularly followed to look for signs and symptoms of torsion of the accessory lobe of the liver.

作者报告一例罕见的脐带疝伴肝副叶夹在羊膜囊内伴桡肢畸形伴旋转不良。肝脏副叶是一种罕见的肝脏解剖变异,通常无症状。肝副叶引起脐环不闭合也是非常罕见的。肝副叶是在胚胎体壁褶皱发育过程中形成的,干扰了脐带环的完全闭合。如果明确诊断为副叶,则应切除。如有疑问,应固定于腹壁,定期随访,寻找肝副叶扭转的体征和症状。
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引用次数: 0
Meconium Peri-orchitis: A Rare Sequela of Intrauterine Intestinal Perforation. 胎粪睾丸周围炎:一种罕见的宫内肠穿孔后遗症。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-06-30 DOI: 10.4103/jiaps.jiaps_108_25
Josy Thomas, Shailesh Solanki, Nitin James Peters, Jai Kumar Mahajan
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引用次数: 0
Hypospadias Penile Skin Landmarks Technique for Preputial Reconstruction in Distal and Mid-penile Hypospadias Undergoing Tubularized Incised Plate Repair. 尿道下裂阴茎皮肤标志技术在阴茎中、远端尿道下裂行管状切开钢板修复后包皮重建中的应用。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-25 DOI: 10.4103/jiaps.jiaps_57_25
Harparkash Singh Miglani, Vikesh Agrawal, Debjani Das

Background: Hypospadias repair has traditionally involved tubularized incised plate urethroplasty, often necessitating circumcision or preputial sacrifice due to dartos flap usage for waterproofing. However, many parents prefer preputial preservation for cultural and aesthetic reasons. No standardized technique currently exists for preputial reconstruction in distal and mid-penile hypospadias. We describe the hypospadias penile skin landmarks (HPS landmarks) technique based on ventral raphe classification and dorsal skin landmarks, a refined surgical approach leveraging natural penile skin creases to facilitate effective preputial reconstruction while maintaining functional and cosmetic outcomes.

Methods: This prospective study, conducted at two centers in India (January 2021-June 2024), included 67 patients (6 months-18 years) with distal and mid-penile hypospadias. A new classification system for ventral raphe and dorsal skin landmarks was proposed to guide preputial reconstruction. Surgical principles involved three key steps: (1) identifying and marking anatomical skin landmarks, (2) selective tissue dissection and preservation, and (3) midline approximation for symmetrical preputial restoration. Functional and cosmetic outcomes, including urethral patency, urinary stream, preputial symmetry, and complications, were assessed postoperatively.

Results: Among 67 cases (52 distal, 15 mid-penile hypospadias), the median age was 14 months, and the mean operative time was 110 ± 18 min. Urethrocutaneous fistula occurred in two patients (2.98%), preputial dehiscence in two (2.98%), and three (4.48%) exhibited persistent dorsal hooding. No cases of glans dehiscence, metal stenosis, or residual chordee were noted. Parental satisfaction was high, with favorable functional and aesthetic outcomes.

Conclusion: The HPS landmarks technique provides a refined surgical approach to preputial reconstruction in distal and mid-penile hypospadias, preserving prepuce integrity while ensuring functional and cosmetic success. By leveraging anatomical skin creases using the described classification, this technique minimizes preputial complications and offers a culturally acceptable alternative for patients desiring preputial preservation. Further long-term studies are warranted to validate its widespread applicability.

背景:传统的尿道下裂修复包括管状切开钢板尿道成形术,由于尿道下裂皮瓣用于防水,通常需要包皮环切或包皮牺牲。然而,出于文化和审美的原因,许多父母更喜欢保留遗嘱。目前还没有标准化的阴茎远端和中端尿道下裂包皮重建技术。我们描述了基于腹侧缝分类和背侧皮肤标记的尿道下裂阴茎皮肤标记(HPS标记)技术,这是一种利用天然阴茎皮肤折痕的精细手术方法,在保持功能和美容效果的同时,促进有效的包皮重建。方法:这项前瞻性研究于2021年1月至2024年6月在印度的两个中心进行,包括67例阴茎远端和中端尿道下裂患者(6个月至18岁)。提出了一种新的中缝腹侧和背侧皮肤标记分类系统,以指导包皮重建。手术原则包括三个关键步骤:(1)识别和标记解剖性皮肤标志,(2)选择性组织剥离和保存,(3)对称包皮修复的中线近似。术后评估功能和美容结果,包括尿道通畅、尿流、包皮对称和并发症。结果:67例(阴茎远端裂52例,中端裂15例)中位年龄14个月,平均手术时间110±18 min。2例(2.98%)出现尿道瘘,2例(2.98%)出现包皮开裂,3例(4.48%)出现持续性背盖。没有发现龟头开裂、金属狭窄或残余脊索的病例。家长满意度高,功能和美观效果良好。结论:HPS标志技术为阴茎远端和中端尿道下裂包皮重建提供了一种精细的手术方法,在保证功能和外观成功的同时,保留了包皮的完整性。通过利用解剖的皮肤折痕使用所描述的分类,该技术最大限度地减少包皮并发症,并为希望包皮保存的患者提供文化上可接受的替代方案。需要进一步的长期研究来验证其广泛的适用性。
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引用次数: 0
Efficacy of Short Duration of Topical Steroids Followed by Adhesiolysis for Management of Preputial Adhesions. 短时间外用类固醇后粘连松解治疗包皮粘连的疗效。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-25 DOI: 10.4103/jiaps.jiaps_10_25
Sumona Bose

Aims: The primary objective was to evaluate the efficacy of a 2-week course of topical corticosteroids and outpatient adhesiolysis in managing preputial adhesions. Secondary objectives included assessing adhesion recurrence rates and monitoring adverse effects related to corticosteroid application and adhesiolysis.

Materials and methods: This prospective observational study was conducted at a tertiary care hospital. Boys presenting with symptoms such as inability to retract the prepuce, ballooning, penile swelling/smegma, urinary symptoms, or history of balanitis were enrolled. Preputial retractability was assessed using the KIKIROS scale. Symptomatic boys with lower KIKIROS grades underwent adhesiolysis during the first visit. Others were advised to apply topical steroids twice daily for 2 weeks, followed by adhesiolysis.

Results: In the 0-<5 years group, the inability to retract prepuce with other symptoms (31%) and ballooning (26%) were common. In the 5-<10 years group, 43.8% had inability to retract the prepuce with associated conditions. In the 10-<17 years group, 64% had inability to retract the prepuce. Post-ointment KIKIROS grading was predominantly 3 in all age groups. After the fifth follow-up, 79.55% of boys who underwent adhesiolysis without ointment achieved KIKIROS 0, compared to 55.39% of those who used ointment.

Conclusion: Topical steroids are helpful, but adhesiolysis alone shows higher efficacy, especially for those with lower initial KIKIROS grades. Reassurance is appropriate for asymptomatic boys under five, while older boys often benefit from intervention. Post-procedure hygiene education and regular follow-up are crucial to minimize recurrence.

目的:主要目的是评估2周疗程的外用皮质类固醇和门诊粘连松解治疗包皮粘连的疗效。次要目的包括评估粘连复发率和监测与皮质类固醇应用和粘连溶解相关的不良反应。材料和方法:本前瞻性观察性研究在一家三级保健医院进行。出现包皮不能缩回、膨胀、阴茎肿胀/包皮肿、泌尿系统症状或有龟头炎史等症状的男孩被纳入研究。使用KIKIROS量表评估包皮可收放性。KIKIROS评分较低的有症状男孩在第一次就诊时进行粘连松解。其他人被建议使用局部类固醇,每天两次,持续2周,然后进行粘连松解。结果:0-结论:局部类固醇是有帮助的,但单独粘连松解效果更好,特别是对于初始KIKIROS分级较低的患者。安抚适用于五岁以下无症状的男孩,而年龄较大的男孩通常从干预中受益。术后卫生教育和定期随访是减少复发的关键。
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引用次数: 0
Appendicolith is Associated with Protracted Abdominal Pain and a High Risk of Appendicular Perforation in Pediatric Appendicitis. 小儿阑尾炎伴持续性腹痛和阑尾穿孔的高风险。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-06-16 DOI: 10.4103/jiaps.jiaps_49_25
Rahul Gupta

Introduction: An appendicolith is a hard fecal concretion that can obstruct the appendix, leading to acute appendicitis. This study aimed to determine the prevalence of appendicoliths in pediatric patients with acute and complicated appendicitis. Secondarily, we aimed to evaluate its association with appendicular perforation peritonitis in pediatric patients.

Materials and methods: This ambispective observational study was conducted from 2018 to 2023 in a pediatric surgery tertiary care teaching institute. The selected patients (n = 181) were those operated on by the author only. Patients were assigned to the appendicolith (n = 80) and no appendicolith groups (n = 101), and clinical features, laboratory data, ultrasound findings, and final diagnosis were compared. Student's t-test and z-score analyses were used to establish statistical significance.

Results: Out of 181 patients, there were 129 males and 52 females (M: F = 2.48:1). The average age of the patients was 7.75 ± 3.35 years. The mean duration of symptoms was 3.62 ± 2.44 days. The mean leukocyte count was 14.24 ± 6.01 × 103/μL, and the mean neutrophil% age was 78.18 ± 9.95. The mean maximal diameter of the appendix was 9.16 ± 2.69 mm. The ultrasound evaluation was highly suggestive of appendicitis in 168 (92.82%) patients. There were 80 (44.2%) patients with appendicolith(s). When appendicolith group and the no appendicolith group were compared, statistically significant differences were present in the age at presentation (6.82 ± 3.39 vs. 8.49 ± 3.15), mean duration of symptoms (4.09 ± 2.9 days vs. 3.25 ± 1.94 days), diarrhea (9, 11.25% vs. 2, 1.98%), anemia (30, 37.5% vs. 18, 17.82%), mean maximal diameter of the appendix (9.99 ± 2.82 mm vs. 8.49 ± 2.38 mm), acute (uncomplicated) appendicitis (13, 16.25% vs. 36, 35.64), and complicated appendicitis (67, 83.75% vs. 65, 64.36%). There was no statistically significant difference in the mean leukocyte count and mean neutrophil% age between the two groups. The maximal diameter of appendicolith ≥5 mm (73) in comparison to the maximal diameter of appendicolith <5 mm (7) was significantly associated with a larger percentage of patients with perforated appendicitis (60, 82.19%) than nonperforated appendicitis (3, 42.86%).

Conclusion: The presence of an appendicolith is associated with prolonged abdominal pain and higher rates of appendicular perforation in pediatric patients with acute appendicitis. The size of the largest appendicolith ≥5 mm is an exacerbating factor for appendicular perforation peritonitis.

阑尾炎是一种坚硬的粪便结块,可阻塞阑尾,导致急性阑尾炎。本研究旨在确定小儿急性和复杂阑尾炎患者阑尾结石的患病率。其次,我们旨在评估其与儿科患者阑尾穿孔性腹膜炎的关系。材料与方法:本双视角观察研究于2018 - 2023年在某儿科外科三级护理教学机构进行。所选患者(n = 181)为作者单独手术的患者。将患者分为阑尾炎组(n = 80)和无阑尾炎组(n = 101),比较临床特征、实验室资料、超声检查结果和最终诊断结果。使用学生t检验和z分数分析来确定统计显著性。结果:181例患者中,男性129例,女性52例(M: F = 2.48:1)。患者平均年龄7.75±3.35岁。平均症状持续时间为3.62±2.44 d。平均白细胞计数14.24±6.01 × 103/μL,平均中性粒细胞%年龄78.18±9.95。阑尾平均最大直径为9.16±2.69 mm。超声检查提示阑尾炎168例(92.82%)。阑尾结石80例(44.2%)。当appendicolith组和无appendicolith组比较,统计学上显著差异存在的年龄表示(6.82±3.39和8.49±3.15),意思是症状的持续时间(4.09±2.9日和3.25±1.94天),腹泻(9 11.25%和2 1.98%),贫血(30 37.5%和18 17.82%),意思是阑尾的最大直径(9.99±2.82毫米和8.49±2.38毫米),急性阑尾炎(简单的)(35.64 13 16.25%比36),和复杂的阑尾炎(67年83.75% vs. 65, 64.36%)。两组患者的平均白细胞计数和平均中性粒细胞年龄差异无统计学意义。结论:小儿急性阑尾炎患者阑尾结石的存在与持续腹痛和较高的阑尾穿孔发生率相关。最大阑尾结石≥5mm是阑尾穿孔性腹膜炎的加重因素。
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引用次数: 0
Clinical Insights and Surgical Management of Pediatric Parathyroid Adenoma: Outcomes and Challenges. 小儿甲状旁腺瘤的临床观察和外科治疗:结果和挑战。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-06-16 DOI: 10.4103/jiaps.jiaps_71_25
A Manasa, Gowri Shankar, Vinay Jadhav

Introduction: Primary hyperparathyroidism (PHPT) is a rare disorder in children, predominantly caused by parathyroid adenoma, often leading to delayed diagnosis and significant morbidity.

Subjects and methods: A prospective analysis of children with PHPT secondary to parathyroid adenoma, study period from 2015 to 2024 at a single institution. Data evaluated included demographics, clinical manifestations, biochemical and radiological features, surgical interventions, and postoperative care.

Results: Six children (4 males, and 2 females) with a mean age of 13.8 years (range 7-17) were evaluated. The mean duration from symptom onset to diagnosis was 3 years. All children presented with musculoskeletal deformities and exhibited elevated serum calcium (mean 12.48 mg/dL) and serum parathyroid hormone levels (1789-2500 picograms per milliliter (pg/mL)). Imaging with ultrasonogram and Isotope scan was successful in confirming the location of parathyroid adenoma with 100% sensitivity. Surgical excision was successful, and all patients developed hungry bone syndrome, requiring calcium supplementation. The mean serum calcium at discharge was 8.68 mg/dL, with no recurrence noted during an average follow-up of 9 years.

Discussion: Pediatric PHPT necessitates a high index of suspicion for timely diagnosis and intervention to prevent development of permanent disabilities. Effective surgical management and postoperative care can significantly enhance patient outcomes.

原发性甲状旁腺功能亢进(PHPT)是一种罕见的儿童疾病,主要由甲状旁腺瘤引起,通常导致诊断延迟和显著的发病率。研究对象和方法:对2015年至2024年单一机构继发于甲状旁腺瘤的PHPT患儿进行前瞻性分析。评估的数据包括人口统计学、临床表现、生化和放射学特征、手术干预和术后护理。结果:6例儿童(男4例,女2例),平均年龄13.8岁(7 ~ 17岁)。从症状出现到诊断的平均时间为3年。所有儿童均表现为肌肉骨骼畸形,血清钙(平均12.48 mg/dL)和血清甲状旁腺激素水平升高(1789-2500皮克/毫升(pg/mL))。超声和同位素扫描对甲状旁腺瘤的定位具有100%的敏感性。手术切除成功,所有患者均出现饥饿骨综合征,需要补钙。出院时平均血钙为8.68 mg/dL,平均随访9年无复发。讨论:儿童PHPT需要高怀疑指数,以便及时诊断和干预,以防止发展为永久性残疾。有效的手术管理和术后护理可以显著提高患者的预后。
{"title":"Clinical Insights and Surgical Management of Pediatric Parathyroid Adenoma: Outcomes and Challenges.","authors":"A Manasa, Gowri Shankar, Vinay Jadhav","doi":"10.4103/jiaps.jiaps_71_25","DOIUrl":"10.4103/jiaps.jiaps_71_25","url":null,"abstract":"<p><strong>Introduction: </strong>Primary hyperparathyroidism (PHPT) is a rare disorder in children, predominantly caused by parathyroid adenoma, often leading to delayed diagnosis and significant morbidity.</p><p><strong>Subjects and methods: </strong>A prospective analysis of children with PHPT secondary to parathyroid adenoma, study period from 2015 to 2024 at a single institution. Data evaluated included demographics, clinical manifestations, biochemical and radiological features, surgical interventions, and postoperative care.</p><p><strong>Results: </strong>Six children (4 males, and 2 females) with a mean age of 13.8 years (range 7-17) were evaluated. The mean duration from symptom onset to diagnosis was 3 years. All children presented with musculoskeletal deformities and exhibited elevated serum calcium (mean 12.48 mg/dL) and serum parathyroid hormone levels (1789-2500 picograms per milliliter (pg/mL)). Imaging with ultrasonogram and Isotope scan was successful in confirming the location of parathyroid adenoma with 100% sensitivity. Surgical excision was successful, and all patients developed hungry bone syndrome, requiring calcium supplementation. The mean serum calcium at discharge was 8.68 mg/dL, with no recurrence noted during an average follow-up of 9 years.</p><p><strong>Discussion: </strong>Pediatric PHPT necessitates a high index of suspicion for timely diagnosis and intervention to prevent development of permanent disabilities. Effective surgical management and postoperative care can significantly enhance patient outcomes.</p>","PeriodicalId":16069,"journal":{"name":"Journal of Indian Association of Pediatric Surgeons","volume":"30 5","pages":"595-599"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12425361/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145064906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cobb's Collar - A Rare Cause of Urinary Obstruction. 柯布氏项圈——一种罕见的尿路阻塞原因。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-16 DOI: 10.4103/jiaps.jiaps_75_25
V V S Chandrasekharam, Khyati Kiran Janapareddy
{"title":"Cobb's Collar - A Rare Cause of Urinary Obstruction.","authors":"V V S Chandrasekharam, Khyati Kiran Janapareddy","doi":"10.4103/jiaps.jiaps_75_25","DOIUrl":"10.4103/jiaps.jiaps_75_25","url":null,"abstract":"","PeriodicalId":16069,"journal":{"name":"Journal of Indian Association of Pediatric Surgeons","volume":"30 5","pages":"685"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12425373/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145064965","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Congenital Extrarenal Malignant Rhabdoid Tumor Involving the Right Shoulder in a Newborn Baby. 新生儿先天性肾外恶性横纹肌样瘤累及右肩1例。
Q3 Medicine Pub Date : 2025-09-01 Epub Date: 2025-05-21 DOI: 10.4103/jiaps.jiaps_33_25
Prashant K Zulpi, K H Ashwini, Rashmi Sajjanshetty, Anita P Javalagi

Congenital extrarenal rhabdoid tumor is a rare soft-tissue tumor, with the most common sites of origin in the genitourinary tract, head and neck regions, and extremities are less commonly involved. Malignant rhabdoid tumors are highly aggressive tumors, and when they develop in utero, the prognosis is even worse, with almost no reports of survival beyond the neonatal period. We present a rare case of congenital extrarenal extracranial rhabdoid tumor on the right shoulder reported at birth and later died after excision due to recurrence of the tumor with distant metastasis.

先天性肾外横纹肌样瘤是一种罕见的软组织肿瘤,最常见的起源部位在泌尿生殖道,头颈部,四肢较少受累。恶性横纹肌瘤是高度侵袭性的肿瘤,当它们在子宫内发展时,预后甚至更差,几乎没有存活过新生儿期的报道。我们报告一例罕见的右肩先天性肾外颅外横纹肌瘤,出生后因肿瘤复发并远处转移而在切除后死亡。
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引用次数: 0
期刊
Journal of Indian Association of Pediatric Surgeons
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