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  1. Article ; Online: Retroperitoneal yolk sac tumour encroaching the liver and adrenal gland with tumour thrombus in cavo-atrial region and hepatic veins.

    Kanneganti, Pujana / Verma, Anju / Kumar, Basant / Nigam, Neha

    BMJ case reports

    2023  Volume 16, Issue 11

    Abstract: Paediatric germ cell tumours (GCT) are rare tumours and are unique because of varied clinical presentation and locations. Yolk sac tumour is the predominant malignant histology and a serum marker; alpha fetoprotein is used to see treatment response and ... ...

    Abstract Paediatric germ cell tumours (GCT) are rare tumours and are unique because of varied clinical presentation and locations. Yolk sac tumour is the predominant malignant histology and a serum marker; alpha fetoprotein is used to see treatment response and recurrent disease. It is extremely rare to find a retroperitoneal GCT with tumour thrombus extending up to the cavo-atrial region with involvement of the hepatic veins. We report a case of retroperitoneal yolk sac tumour (RPYST) with extension to the liver and right adrenal gland along with tumour thrombus in the inferior vena cava and in the right and middle hepatic veins. The child was operated after satisfactory response to chemotherapy. Excision of the tumour along with the right adrenal gland and around 5 cm of retro-hepatic caval resection was done. Inferior vena cava resection was tolerated without reconstruction. Currently child is disease-free and symptom-free at 22 months of follow-up with normal serum marker.
    MeSH term(s) Humans ; Child ; Hepatic Veins ; Endodermal Sinus Tumor/complications ; Endodermal Sinus Tumor/surgery ; Endodermal Sinus Tumor/pathology ; Atrial Fibrillation ; Thrombosis/etiology ; Thrombosis/surgery ; Thrombosis/pathology ; Vena Cava, Inferior/surgery ; Vena Cava, Inferior/pathology ; Liver/surgery ; Liver/pathology ; Adrenal Glands/diagnostic imaging ; Adrenal Glands/surgery ; Adrenal Glands/pathology ; Neoplasms, Germ Cell and Embryonal/pathology
    Language English
    Publishing date 2023-11-03
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2023-255968
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Extensive intramural calcification in neonatal ileal atresia: An unusual finding.

    Prasad, Pallavi / Radha, Paturu / Kumar, Basant / Kanneganti, Pujana

    Indian journal of pathology & microbiology

    2023  

    Language English
    Publishing date 2023-07-26
    Publishing country India
    Document type Journal Article
    ZDB-ID 197621-7
    ISSN 0974-5130 ; 0377-4929
    ISSN (online) 0974-5130
    ISSN 0377-4929
    DOI 10.4103/ijpm.ijpm_890_22
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Laparoscopic Transperitoneal Adrenalectomy for Adrenal Tumors in Children: Technical Considerations and Surgical Experience.

    Mandelia, Ankur / Mayilvaganan, Sabaretnam / Naik, Prathibha B / Kanneganti, Pujana

    Journal of laparoendoscopic & advanced surgical techniques. Part A

    2023  Volume 34, Issue 2, Page(s) 189–198

    Abstract: Aims: ...

    Abstract Aims:
    MeSH term(s) Male ; Female ; Humans ; Child ; Middle Aged ; Adrenalectomy/methods ; Retrospective Studies ; Laparoscopy/methods ; Adrenal Gland Neoplasms/surgery ; Adrenal Gland Neoplasms/pathology ; Adrenal Glands/pathology
    Language English
    Publishing date 2023-10-20
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1381909-4
    ISSN 1557-9034 ; 1092-6429
    ISSN (online) 1557-9034
    ISSN 1092-6429
    DOI 10.1089/lap.2023.0160
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Giant renal parapelvic cyst with pelvi-ureteric junction obstruction in an infant: challenges in diagnosis and laparoscopic management.

    Kapoor, Rohit / Mandelia, Ankur / Verma, Anju / Kanneganti, Pujana

    BMJ case reports

    2022  Volume 15, Issue 5

    Abstract: Renal parapelvic cysts (RPC) have an incidence of approximately 1%-3% in the general population. However, they rarely present in children with only two cases reported in literature. RPC are often misdiagnosed as it is difficult to distinguish them from ... ...

    Abstract Renal parapelvic cysts (RPC) have an incidence of approximately 1%-3% in the general population. However, they rarely present in children with only two cases reported in literature. RPC are often misdiagnosed as it is difficult to distinguish them from hydronephrosis on preoperative imaging. We report a case of an infant with a giant RPC with associated pelvi-ureteric junction obstruction, who was managed successfully with laparoscopic complete excision of RPC and dismembered pyeloplasty. In our report, we discuss the challenges faced in the diagnosis and surgical management of this unusual case.
    MeSH term(s) Child ; Cysts/diagnosis ; Cysts/diagnostic imaging ; Female ; Humans ; Hydronephrosis/congenital ; Hydronephrosis/diagnostic imaging ; Hydronephrosis/etiology ; Infant ; Kidney Diseases, Cystic/surgery ; Kidney Pelvis/diagnostic imaging ; Kidney Pelvis/surgery ; Laparoscopy/methods ; Male ; Multicystic Dysplastic Kidney ; Ureteral Obstruction/diagnostic imaging ; Ureteral Obstruction/etiology
    Language English
    Publishing date 2022-05-11
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1757-790X
    ISSN (online) 1757-790X
    DOI 10.1136/bcr-2022-249548
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Bronchial Carcinoid Tumor in an Adolescent Female: Diagnosis and Management by a Multi-Disciplinary Team.

    Kapoor, Rohit / Mandelia, Ankur / Farzana, Nayab / Nigam, Neha / Dabadghao, Preeti / Sharma, Shyamendra Pratap / Kanneganti, Pujana / Pande, Shantanu

    Journal of Indian Association of Pediatric Surgeons

    2022  Volume 27, Issue 4, Page(s) 500–502

    Abstract: Bronchial carcinoid is the most common primary malignant lung tumor in children; however, it remains a very rare diagnosis due to the overall low incidence of childhood lung malignancies. We report a case of a 17-year-old girl with respiratory symptoms ... ...

    Abstract Bronchial carcinoid is the most common primary malignant lung tumor in children; however, it remains a very rare diagnosis due to the overall low incidence of childhood lung malignancies. We report a case of a 17-year-old girl with respiratory symptoms who was initially misdiagnosed as a case of COVID pneumonia. She was later detected to have a right mainstem bronchial carcinoid which was managed successfully by a multi-disciplinary team.
    Language English
    Publishing date 2022-07-26
    Publishing country India
    Document type Case Reports
    ZDB-ID 2164528-0
    ISSN 1998-3891 ; 0971-9261
    ISSN (online) 1998-3891
    ISSN 0971-9261
    DOI 10.4103/jiaps.jiaps_132_21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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