scholarly journals A Rare Case of Genital Malformation with Omphalocele, Exstrophy of Bladder, Imperforate Anus and Spinal Defect Complex-Autopsy Findings

2017 ◽  
Author(s):  
K. Mamatha
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Defect Complex ◽  
Autopsy Findings ◽  
Genital Malformation

scholarly journals A Rare Case of Omphalocele, Exstrophy of Bladder, Imperforate Anus and Spinal Defect Complex with Genital Anomalies in a Term Neonate

2021 ◽  
Vol 18 (3) ◽  
Author(s):  
Deepali Ambike ◽  
Abhijeet Byale ◽  
Rijwana Sayyad ◽  
Vinit Rathod ◽  
Komal Bijarniya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Defect Complex

scholarly journals Systemic congenital lymphangiomatosis

1996 ◽  
Vol 114 (5) ◽  
pp. 1278-1281 ◽  
Author(s):  
Ligia Maria Suppo de Souza ◽  
Maria Regina Bentlin ◽  
Eliana Souto de Abreu ◽  
Carlos Eduardo Bacchi
Keyword(s):  
Young Adults ◽  
Respiratory Failure ◽  
Rare Disease ◽  
Poor Prognosis ◽  
Rare Case ◽  
Soft Tissues ◽  
Lymphatic Channel ◽  
Autopsy Findings ◽  
Children And Young Adults ◽  
Cervical Area

Systemic lymphangiomatosis is a rare disease characterized by the exageration of lymphatic channel proliferation, occurring in children and young adults. We describe an extremely rare case of congenital systemic lymphangiomatosis in a newborn who had ascitis and respiratory failure develop immediately after delivery. Death occurred during the first hour of life. Autopsy findings showed numerous cysts in soft tissues of the cervical area, mediastinum and diaphragm, and several other organs including the liver, spleen, thyroid and kidneys. The severe and diffuse involvement with cysts in both lungs by lymphangiomatosis was associated with poor prognosis and death in our case.

scholarly journals Autopsy Findings of Oleander Poisoning – Report of A Rare Case

2020 ◽  
Vol 08 (04) ◽  
pp. 485-487
Author(s):  
Dr. Nirjhar Saha ◽  
Dr. Chandan Bandopadhyay ◽  
Dr. Biswajit Sukul
Keyword(s):  
Rare Case ◽  
Autopsy Findings

scholarly journals A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

2014 ◽  
Vol 12 (2) ◽  
pp. 234-236
Author(s):  
Kleiton Gabriel Ribeiro Yamaçake ◽  
Amilcar Martins Giron ◽  
Uenis Tannuri ◽  
Miguel Srougi
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Imperforate Anus ◽  
Rare Case ◽  
Coloanal Anastomosis ◽  
Histopathological Examination ◽  
Congenital Clubfoot ◽  
Anorectal Anomaly ◽  
Male Neonate ◽  
Nonpalpable Testis

A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.

Rectal adenocarcinoma following imperforate anus: A rare case report

2020 ◽  
pp. 252-254
Author(s):  
Sarah Khan ◽  
Hina Khan ◽  
Jan Agha ◽  
Khursheed Samo ◽  
Mujeeb Abbasi ◽  
...  
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
Rare Case ◽  
Rectal Adenocarcinoma ◽  
Rare Case Report

scholarly journals A RARE CASE OF HETEROTAXIA: FETAL AUTOPSY FINDINGS

2020 ◽  
Vol 28 (1) ◽  
Author(s):  
Daisy Dwivedi ◽  
Bal Chander
Keyword(s):  
Rare Case ◽  
Mirror Image ◽  
First Year ◽  
Male Fetus ◽  
Fetal Autopsy ◽  
Autopsy Findings ◽  
Situs Solitus ◽  
The Right ◽  
Thoracic And Abdominal ◽  
Asymmetrically Distributed

Visceral organs are asymmetrically distributed in thoracic and abdominal cavities but there is definite left right orientation along the midline. At times there may be disturbance of the same resulting from malrotation and/or movement during embryological development. We are presenting autopsy findings of a 20 weeks old male fetus wherein the stomach along with spleen and pancreas are on the right side. Rest of the thoracoabdominal viscera are in the anatomically correct locations. Such cases qualify for heterotaxia, denoting status somewhere between situs solitus which is the normal placement of organs and situs inversus which denotes mirror image of solitus. Heterotaxia can have a range of features. Such cases usually come to light within first year of birth but some cases remain asymptomatic till adulthood and are diagnosed incidentally. This article discusses the nomenclature with diagnostic criteria and points out the lacunae which make the present case difficult to classify.

scholarly journals A RARE CASE OF BIFID PENIS WITH IMPERFORATE ANUS

2014 ◽  
Vol 3 (48) ◽  
pp. 11614-11616
Author(s):  
Sharan Deshmukh ◽  
Shrikant S W ◽  
Sharangouda Patil ◽  
Harilal Naik M L
Keyword(s):  
Imperforate Anus ◽  
Rare Case

scholarly journals Complete Penoscrotal Transposition with Other Extragenital Anomalies in a Neonate Delivered at Term

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Ali Mahamudu Ayamba ◽  
Raymond Saa-Eru Maalman ◽  
Yaw Otchere Donkor ◽  
John Noah Anyorigiya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Cardiac Malformation ◽  
Facial Deformity ◽  
Antenatal Services ◽  
Penoscrotal Transposition

A complete penoscrotal transposition (CPST) is a very uncommon congenital maldevelopment that is always associated with other abnormal body variations (malformations). We report a rare case of a term neonate delivered with CPST, which had a flaccid penis and an intact scrotum with unilateral limb and digital deformity, imperforate anus, cardiac malformation a facial deformity. Neonate died two hours after delivery. The foetal abnormality was not detected through routine antenatal services received by the mother.

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