Use and outcomes of kidneys from donors with renal angiomyolipoma: A systematic review.

Donor kidney transplant renal angiomyolipoma renal transplantation transplantation

Journal

Urology annals
ISSN: 0974-7796
Titre abrégé: Urol Ann
Pays: India
ID NLM: 101510823

Informations de publication

Date de publication:
Historique:
received: 23 02 2020
accepted: 25 08 2020
entrez: 26 4 2021
pubmed: 27 4 2021
medline: 27 4 2021
Statut: ppublish

Résumé

Renal angiomyolipoma (AML) is the most frequent mesenchymal tumor of the kidney. Although there is a rare possibility of malignant transformation of AML, this risk has not been studied in immunosuppressed patients. The safety of donors with AML and their kidney transplant recipients has not been well established. A literature search was conducted utilizing MEDLINE, EMBASE, and Cochrane databases from inception through May 15, 2018 (updated on October 2019). We included studies that reported the outcomes of kidney donors with AML or recipients of donor with AML. The protocol for this meta-analysis is registered with PROSPERO (International Prospective Register of Systematic Reviews; no. CRD42018095157). Fourteen studies with a total of 16 donors with AML were identified. None of the donors had a diagnosis of tuberous sclerosis complex (TSC), pulmonary lymphangioleiomyomatosis (LAM), or epithelioid variant of AML. Donor age ranged from 35 to 77 years, and recipient age ranged from 27 to 62 years. Ninety-two percent of the donors were female. Only 8% were deceased donor renal transplant. The majority underwent These findings are reassuring for the safety of donors with AML (without TSC or LAM) as well as their recipients without evidence of malignant transformation of AML. As such, this can also positively impact the donor pool by increasing the number of available kidneys.

Sections du résumé

BACKGROUND BACKGROUND
Renal angiomyolipoma (AML) is the most frequent mesenchymal tumor of the kidney. Although there is a rare possibility of malignant transformation of AML, this risk has not been studied in immunosuppressed patients. The safety of donors with AML and their kidney transplant recipients has not been well established.
METHODS METHODS
A literature search was conducted utilizing MEDLINE, EMBASE, and Cochrane databases from inception through May 15, 2018 (updated on October 2019). We included studies that reported the outcomes of kidney donors with AML or recipients of donor with AML. The protocol for this meta-analysis is registered with PROSPERO (International Prospective Register of Systematic Reviews; no. CRD42018095157).
RESULTS RESULTS
Fourteen studies with a total of 16 donors with AML were identified. None of the donors had a diagnosis of tuberous sclerosis complex (TSC), pulmonary lymphangioleiomyomatosis (LAM), or epithelioid variant of AML. Donor age ranged from 35 to 77 years, and recipient age ranged from 27 to 62 years. Ninety-two percent of the donors were female. Only 8% were deceased donor renal transplant. The majority underwent
CONCLUSION CONCLUSIONS
These findings are reassuring for the safety of donors with AML (without TSC or LAM) as well as their recipients without evidence of malignant transformation of AML. As such, this can also positively impact the donor pool by increasing the number of available kidneys.

Identifiants

pubmed: 33897168
doi: 10.4103/UA.UA_14_20
pii: UA-13-67
pmc: PMC8052899
doi:

Types de publication

Journal Article

Langues

eng

Pagination

67-72

Informations de copyright

Copyright: © 2021 Urology Annals.

Déclaration de conflit d'intérêts

There are no conflicts of interest.

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Auteurs

Desiree Garcia Anton (DG)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Karthik Kovvuru (K)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Swetha R Kanduri (SR)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Narothama Reddy Aeddula (NR)

Department of Medicine, Division of Nephrology, Deaconess Health System, Evansville, IN, USA.

Tarun Bathini (T)

Department of Internal Medicine, University of Arizona, Tucson, AZ, USA.

Charat Thongprayoon (C)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Wisit Kaewput (W)

Department of Military and Community Medicine, Phramongkutklao College of Medicine, Bangkok, Thailand.

Karn Wijarnpreecha (K)

Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Mayo Clinic, Jacksonville, Florida, USA.

Kanramon Watthanasuntorn (K)

Department of Internal Medicine, Bassett Medical Center, Cooperstown, New York, USA.

Sohail Abdul Salim (SA)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Praise Matemavi (P)

Department of Department of Transplant and Hepatobiliary Surgery, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Pradeep Vaitla (P)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Franco Cabeza Rivera (FC)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Wisit Cheungpasitporn (W)

Department of Internal Medicine, Division of Nephrology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Classifications MeSH