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1.
Archives of Plastic Surgery ; : 470-474, 2019.
Article in English | WPRIM | ID: wpr-762859

ABSTRACT

Congenital absent sternum is a rare birth defect that requires early intervention for optimal long-term outcomes. Descriptions of the repair of absent sternum are limited to case reports, and no preferred method for management has been described. Herein, we describe the use of porcine acellular dermal matrix to reconstruct the sternum of an infant with sternal infection following attempted repair using synthetic mesh. The patient was a full-term male with trisomy 21, agenesis of corpus callosum, ventricular septal defect, patent ductus arteriosus, right-sided aortic arch, and congenital absence of sternum with no sternal bars. Following removal of the infected synthetic mesh, negative pressure wound therapy with instillation was used to manage the open wound and provide direct antibiotic therapy. When blood C-reactive protein levels declined to ≤2 mg/L, the sternum was reconstructed using porcine acellular dermal matrix. At 21 months postoperative, the patient demonstrated no respiratory issues. Physical examination and computed tomography imaging identified good approximation of the clavicular heads and sternal cleft and forward curvature of the ribs. This case illustrates the benefits of negative pressure wound therapy and acellular dermal matrix for the reconstruction of absent sternum in the context of infected sternal surgical site previously repaired with synthetic mesh.


Subject(s)
Humans , Infant , Male , Acellular Dermis , Agenesis of Corpus Callosum , Aorta, Thoracic , C-Reactive Protein , Congenital Abnormalities , Down Syndrome , Ductus Arteriosus, Patent , Early Intervention, Educational , Head , Heart Septal Defects, Ventricular , Methods , Negative-Pressure Wound Therapy , Physical Examination , Ribs , Sternum , Surgical Mesh , Thoracic Surgery , Wounds and Injuries
2.
Indian J Pathol Microbiol ; 2007 Oct; 50(4): 819-21
Article in English | IMSEAR | ID: sea-73437

ABSTRACT

Well differentiated villoglandular adenocarcinoma of uterine cervix is a rare tumour which usually occurs in young women. It is considered to be an indolent tumour with favorable prognosis and most of them were treated by conservative procedures. We report a 35 year old lady who came with complaints of 3 months amenorrhoea and an episode of spontaneous bleeding. Urine pregnancy test was negative. Physical examination revealed a cervical polyp. Histopathological findings were consistent with villoglandular papillary adenocarcinoma associated with high grade cervical intraepithelial neoplasia (CIN-3). Left parametrial and left ureteral involvement, proved by biopsy, causing left hydroureteronephrosis was detected. The patient was thus found to be in an advanced stage, stage- III b (FIGO). The patient is currently undergoing radiotherapy. A review of literature showed that only occasional cases showing disease spread have been reported, suggesting caution in the management and regular follow up of the patient.


Subject(s)
Adenocarcinoma, Papillary/complications , Adnexa Uteri/pathology , Adult , Antineoplastic Agents/therapeutic use , Uterine Cervical Dysplasia/complications , Cisplatin/therapeutic use , Female , Humans , Hydronephrosis , Polyps , Ureter/pathology , Uterine Cervical Neoplasms/complications
3.
Indian J Pathol Microbiol ; 2006 Apr; 49(2): 263-4
Article in English | IMSEAR | ID: sea-75217

ABSTRACT

Benign mucinous metaplasia of the prepuce is a rare and under recognized entity which can easily be mistaken for extramammary Paget's disease. It is characterized by the presence of benign mucin containing cells in the squamous epithelium. To the best of our knowledge only 6 such cases have been documented in the literature. We would like to report the first case in our country.


Subject(s)
Diagnosis, Differential , Humans , Male , Metaplasia/metabolism , Middle Aged , Mucins/metabolism , Paget Disease, Extramammary/diagnosis , Penile Diseases/diagnosis , Penis/metabolism
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