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  1. Article ; Online: Aux sources de la compréhensionde la maladie rénale chronique.

    Vergnaud, Paul / Cohen, Camille / Isnard, Pierre

    Medecine sciences : M/S

    2023  Volume 39, Issue 3, Page(s) 265–270

    Abstract: Chronic kidney disease (CKD) is a global health problem affecting almost 15% of the population worldwide. After renal injury, there is a nephron loss and remaining nephrons ensure the glomerular filtration rate (GFR) with compensatory hyperplasia and ... ...

    Title translation Towards understanding chronic kidney disease.
    Abstract Chronic kidney disease (CKD) is a global health problem affecting almost 15% of the population worldwide. After renal injury, there is a nephron loss and remaining nephrons ensure the glomerular filtration rate (GFR) with compensatory hyperplasia and hypertrophy: This is called the nephron reduction. After nephron reduction, renal function will gradually decline and lead to chronic end-stage renal failure. Whatever the initial cause of the renal injury, recent data suggest there are common molecular mechanisms at the origin of CKD progression. Moreover, the renal lesions are very reproducible with glomerulosclerosis, tubular atrophy and partial epithelio-mesenchymal transition, interstitial fibrosis and vascular abnormalities. The physiopathology of CKD progression is unclear but some hypotheses have been described: i) the nephron "overwork", supported by recent works showing that the nephron reduction leads to hyperfiltration by the remaining nephrons and the stability of the GFR; ii) the "podocyte adaptation" theory, reflected by the importance of the podocytopathy in CKD progression and the crucial role of residual proteinuria in renal lesion development; iii) the activation of EGFR signaling pathways in surgical nephron reduction model and its involvement in CKD progression. Finally, CKD progression remains poorly understood and further studies will be necessary to discover new CKD molecular pathways and to develop new therapeutic insight in CKD management.
    MeSH term(s) Humans ; Kidney ; Renal Insufficiency, Chronic/complications ; Nephrons ; Proteinuria ; Glomerular Filtration Rate/physiology ; Podocytes ; Disease Progression
    Language French
    Publishing date 2023-03-21
    Publishing country France
    Document type English Abstract ; Journal Article
    ZDB-ID 632733-3
    ISSN 1958-5381 ; 0767-0974
    ISSN (online) 1958-5381
    ISSN 0767-0974
    DOI 10.1051/medsci/2023033
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Case | Crescentic glomerulonephritis in a kidney transplant recipient.

    Isnard, Pierre / Tang, Ellie / Mroue, Ahmad / Letavernier, Emmanuel / Verine, Jérôme

    Kidney international

    2023  Volume 103, Issue 6, Page(s) 1205–1206

    MeSH term(s) Humans ; Kidney Transplantation/adverse effects ; Kidney ; Glomerulonephritis/diagnosis ; Glomerulonephritis, Membranoproliferative ; Acute Disease
    Language English
    Publishing date 2023-04-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2023.01.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Histoséminaire de la Société française de pathologie « Quand les tumeurs pédiatriques et adultes se rejoignent » Cas n

    Bruneau, Julie / Isnard, Pierre / Morcrette, Guillaume / Couronné, Lucile / Molina, Thierry-Jo

    Annales de pathologie

    2023  Volume 43, Issue 4, Page(s) 338–341

    Title translation Histoseminar: "When paediatric and adult tumours converge" Case 7.
    MeSH term(s) Adult ; Child ; Humans ; Neoplasms
    Language French
    Publishing date 2023-05-01
    Publishing country France
    Document type Case Reports ; Journal Article
    ZDB-ID 225720-8
    ISSN 0242-6498
    ISSN 0242-6498
    DOI 10.1016/j.annpat.2023.04.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Autoimmune Phenomenon Associated With Posttransplant Lymphoproliferative Disorder.

    Isnard, Pierre / Huynh, Tony / Lhermitte, Ludovic / Hermine, Olivier / Thervet, Eric / Molina, Thierry Jo

    Kidney international reports

    2023  Volume 9, Issue 3, Page(s) 725–729

    Language English
    Publishing date 2023-12-29
    Publishing country United States
    Document type Case Reports
    ISSN 2468-0249
    ISSN (online) 2468-0249
    DOI 10.1016/j.ekir.2023.12.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A 39 year-old man with acroparesthesia and uncommon renal arterial lesions. What is the diagnosis?

    Creon, Antoine / Ferriere, Elsa / Rabant, Marion / Van Huyen, Jean-Paul Duong / Isnard, Pierre

    Journal of nephrology

    2022  Volume 36, Issue 1, Page(s) 241–243

    MeSH term(s) Male ; Humans ; Adult ; Kidney/diagnostic imaging ; Kidney/pathology ; Fabry Disease/pathology ; alpha-Galactosidase
    Chemical Substances alpha-Galactosidase (EC 3.2.1.22)
    Language English
    Publishing date 2022-02-23
    Publishing country Italy
    Document type Case Reports ; Journal Article
    ZDB-ID 1093991-x
    ISSN 1724-6059 ; 1120-3625 ; 1121-8428
    ISSN (online) 1724-6059
    ISSN 1120-3625 ; 1121-8428
    DOI 10.1007/s40620-022-01277-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Mycobacterium canettii Tuberculosis Lymphadenopathy in a 3-Year-old Child.

    Faury, Hélène / Stanzelova, Anna / Ferroni, Agnès / Belhous, Kahina / Morand, Philippe / Toubiana, Julie / Bille, Emmanuelle / Isnard, Pierre / Simon, François / Lécuyer, Hervé

    The Pediatric infectious disease journal

    2023  Volume 42, Issue 9, Page(s) e345–e347

    Abstract: A 3-year-old male originating from Djibouti presented with a cervical mass evolving for 2 months. Tuberculous lymphadenopathy was suspected based on biopsy results, and he improved quickly on standard antituberculous quadritherapy. Subsequently some ... ...

    Abstract A 3-year-old male originating from Djibouti presented with a cervical mass evolving for 2 months. Tuberculous lymphadenopathy was suspected based on biopsy results, and he improved quickly on standard antituberculous quadritherapy. Subsequently some features of the mycobacterium that grew in culture were unusual. The isolate was eventually identified as Mycobacterium canettii , a peculiar species of the Mycobacterium tuberculosis complex.
    MeSH term(s) Male ; Humans ; Child, Preschool ; Mycobacterium ; Tuberculosis, Lymph Node/diagnosis ; Tuberculosis, Lymph Node/drug therapy ; Djibouti ; Lymphadenopathy ; Mycobacterium tuberculosis
    Language English
    Publishing date 2023-05-26
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 392481-6
    ISSN 1532-0987 ; 0891-3668
    ISSN (online) 1532-0987
    ISSN 0891-3668
    DOI 10.1097/INF.0000000000003983
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Stiripentol and Lumasiran as a Rescue Therapy for Oxalate Nephropathy Recurrence After Kidney Transplantation in an Adult Patient With Primary Hyperoxaluria Type 1.

    Lombardi, Yannis / Isnard, Pierre / Chavarot, Nathalie / Chauvet, Sophie / Martinez, Frank / Thervet, Éric / Anglicheau, Dany / Karras, Alexandre

    American journal of kidney diseases : the official journal of the National Kidney Foundation

    2023  Volume 82, Issue 1, Page(s) 113–116

    Abstract: Primary hyperoxaluria type 1 is a rare cause of kidney failure. Stiripentol, an inhibitor of lactate dehydrogenase A, and lumasiran, a small interfering RNA targeting glycolate oxidase, have been proposed as therapeutic options, but clinical data are ... ...

    Abstract Primary hyperoxaluria type 1 is a rare cause of kidney failure. Stiripentol, an inhibitor of lactate dehydrogenase A, and lumasiran, a small interfering RNA targeting glycolate oxidase, have been proposed as therapeutic options, but clinical data are scarce, especially in adults and transplanted patients. We describe the case of a 51-year-old patient with a biopsy-proven recurrence of oxalate nephropathy after a kidney-only transplantation. He received stiripentol and lumasiran without adverse events. Fourteen months after transplantation, graft function, serum, and urinary oxalate levels have remained stable, and kidney biopsy showed a complete regression of oxalate crystals. Further studies are needed to assess whether this strategy is effective and could replace liver-kidney transplantation.
    MeSH term(s) Male ; Humans ; Adult ; Middle Aged ; Kidney Transplantation/adverse effects ; Hyperoxaluria, Primary/complications ; Hyperoxaluria, Primary/surgery ; Hyperoxaluria/etiology ; RNA, Small Interfering ; Renal Insufficiency/etiology ; Oxalates
    Chemical Substances stiripentol (R02XOT8V8I) ; lumasiran (RZT8C352O1) ; RNA, Small Interfering ; Oxalates
    Language English
    Publishing date 2023-01-21
    Publishing country United States
    Document type Case Reports
    ZDB-ID 604539-x
    ISSN 1523-6838 ; 0272-6386
    ISSN (online) 1523-6838
    ISSN 0272-6386
    DOI 10.1053/j.ajkd.2022.12.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Cutaneous Granulomatosis Revealing Whipple’s Disease: Value of Tropheryma whipplei Polymerase Chain Reaction Assay for the Diagnosis

    Zayet, Souheil / Isnard, Pierre / Bustamante, Jacinta / Boutboul, David / Abroug, Sarra / Belfeki, Nabil

    Pathogens. 2021 Nov. 05, v. 10, no. 11

    2021  

    Abstract: Whipple’s Disease is a rare systemic infectious disease caused by the ubiquitous actinomycetes Tropheryma whipplei (T. whipplei). We report herein a rare case of a cutaneous granulo matosis with hypercalcemia as an unusual presenting feature of Whipple’s ...

    Abstract Whipple’s Disease is a rare systemic infectious disease caused by the ubiquitous actinomycetes Tropheryma whipplei (T. whipplei). We report herein a rare case of a cutaneous granulo matosis with hypercalcemia as an unusual presenting feature of Whipple’s disease. The diagnosis of the bacteria was obtained from skin and inguinal lymph node biopsy (16 rDNA PCR screening and histological examination using PAS staining). T. whipplei was also identified on saliva and stool specimens, using specific PCR and colonic biopsies. Treatment with hydroxychloroquine and doxycycline allowed a rapid resolution of symptoms with a complete recovery.
    Keywords Tropheryma ; biopsy ; doxycycline ; histology ; hypercalcemia ; infectious diseases ; lymph nodes ; polymerase chain reaction ; saliva
    Language English
    Dates of publication 2021-1105
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article
    ZDB-ID 2695572-6
    ISSN 2076-0817
    ISSN 2076-0817
    DOI 10.3390/pathogens10111438
    Database NAL-Catalogue (AGRICOLA)

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  9. Article: Cutaneous Granulomatosis Revealing Whipple's Disease: Value of

    Zayet, Souheil / Isnard, Pierre / Bustamante, Jacinta / Boutboul, David / Abroug, Sarra / Belfeki, Nabil

    Pathogens (Basel, Switzerland)

    2021  Volume 10, Issue 11

    Abstract: Whipple's Disease is a rare systemic infectious disease caused by the ubiquitous ... ...

    Abstract Whipple's Disease is a rare systemic infectious disease caused by the ubiquitous actinomycetes
    Language English
    Publishing date 2021-11-05
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2695572-6
    ISSN 2076-0817
    ISSN 2076-0817
    DOI 10.3390/pathogens10111438
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Pathologie de la transplantation cardiaque : où en est-on 15 ans et 7 ans après les documents de consensus sur le rejet cellulaire et humoral.

    Rabant, Marion / Coutance, Guillaume / Isnard, Pierre / Duong-Van-Huyen, Jean-Paul

    Annales de pathologie

    2021  Volume 41, Issue 1, Page(s) 38–49

    Abstract: Pathology is still the gold standard for the diagnosis of rejection in heart transplantation. During the last decade, molecular pathology has emerged as a powerful tool for the understanding of the processes implicated in allograft rejection. ... ...

    Title translation Pathology of heart transplantation: Where are we now?
    Abstract Pathology is still the gold standard for the diagnosis of rejection in heart transplantation. During the last decade, molecular pathology has emerged as a powerful tool for the understanding of the processes implicated in allograft rejection. Transcriptomic analysis of the allograft may also help the pathologist for diagnosis and accurate classification of rejection. This review will describe the recent advances and perspectives of molecular pathology in the field of heart transplantation.
    MeSH term(s) Graft Rejection/diagnosis ; Heart Transplantation ; Humans ; Transplantation, Homologous
    Language French
    Publishing date 2021-01-04
    Publishing country France
    Document type Journal Article ; Review
    ZDB-ID 225720-8
    ISSN 0242-6498
    ISSN 0242-6498
    DOI 10.1016/j.annpat.2020.12.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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