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1.
Leukemia ; 31(1): 123-129, 2017 01.
Article in English | MEDLINE | ID: mdl-27435002

ABSTRACT

We retrospectively reviewed 49 patients with light chain (LC) Fanconi syndrome (FS). Patients presented with chronic kidney disease (median estimated glomerular filtration rate (eGFR) of 33 ml/min/1.73 m2) and tubular proteinuria. All patients tested had elevated fractional excretion of phosphate, uric acid, generalized aminoaciduria and/or normoglycemic glycosuria. Thirty-eight patients had monoclonal gammopathy of renal significance and eleven patients had an overt hematological malignancy. The monoclonal LC isotype was kappa in 46/49 cases. Kidney biopsy in 39 patients showed various proximal tubular lesions and characteristic LC intracytoplasmic crystalline inclusions in 24 patients. Forty-two patients received chemotherapy. Patients with plasma cell proliferation (n=38) received bortezomib-based regimens (n=11), immunomodulatory agents (n=7) or alkylating agents (n=6). High-dose melphalan (HDM) followed by autologous stem cell transplantation was performed in 14 patients. Hematological response was obtained in 90% of evaluable patients, assessed on serum free light chains (FLC). GFR remained stable as long as hematological response was maintained and declined when serum FLC level rebounded. Improvement in proximal tubule function occurred in 13 patients. In patients with LC-associated FS, chemotherapy using HDM and/or new generation anti-myeloma agents can stabilize renal function and improve proximal tubule function. Serum FLC should be used to assess the hematological response, related to renal outcome.


Subject(s)
Fanconi Syndrome/therapy , Immunoglobulin Light Chains , Adult , Aged , Aged, 80 and over , Combined Modality Therapy , Female , Hematologic Neoplasms/therapy , Humans , Kidney Diseases , Male , Middle Aged , Paraproteinemias/pathology , Paraproteinemias/therapy , Retrospective Studies , Treatment Outcome
2.
Rev Med Interne ; 35(4): 222-30, 2014 Apr.
Article in French | MEDLINE | ID: mdl-23743480

ABSTRACT

PURPOSE: Myeloproliferative neoplasms (MPN) are hematological disorders characterized by clonal expansion of one or more medullary lines. Renal complications are rare, chiefly as acute renal failure. Glomerular involvement is exceptional METHODS: We report on a retrospective multicenter case series of eight patients who presented with a glomerulopathy (GP) associated with MPN RESULTS: All GP were revealed by a major proteinuria frequently associated with nephrotic syndrome and oedema. Histology was mainly characterized by lesions of focal segmental glomerulosclerosis associated with increased mesangial cellularity. The pathophysiology is still unclear but platelet-derived growth factor (PDGF) and transforming growth factor-ß (TGF-ß), which play a central role in the MPN may be involved. A majority of patients developed chronic renal failure despite of a therapy intended to block the renin-angiotensin system CONCLUSION: Monitoring of proteinuria during the follow-up of MPN would allow earlier diagnosis of renal involvement. Further studies on a larger scale are needed to specify the pathophysiological mechanisms involved and the management of these complications.


Subject(s)
Kidney Diseases/etiology , Myeloproliferative Disorders/complications , Acute Kidney Injury/diagnosis , Acute Kidney Injury/epidemiology , Acute Kidney Injury/etiology , Acute Kidney Injury/pathology , Adult , Aged , Aged, 80 and over , Biopsy , Female , Humans , Kidney Diseases/diagnosis , Kidney Diseases/epidemiology , Kidney Diseases/pathology , Kidney Glomerulus/pathology , Male , Middle Aged , Myeloproliferative Disorders/diagnosis , Myeloproliferative Disorders/epidemiology , Retrospective Studies
3.
Transpl Infect Dis ; 11(4): 359-62, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19497046

ABSTRACT

Rhodococcus equi is a bacterial pathogen of domestic animals that can infect immunocompromised patients, especially those with impaired cellular immunity, such as transplant recipients. No standard treatment has been established, but therapy must be prolonged, as relapses are common and can occur at the initial site or distant locations. Here we report a case of R. equi-associated pulmonary abscess in a renal transplant recipient successfully treated with a combination of carbapenem and teicoplanin. This combination was shown to be synergistic. It has minimal side effects in transplant recipients and appears to be an effective initial treatment for this severe infection.


Subject(s)
Actinomycetales Infections/drug therapy , Anti-Bacterial Agents/therapeutic use , Carbapenems/therapeutic use , Kidney Transplantation/adverse effects , Pneumonia, Bacterial/drug therapy , Rhodococcus equi/drug effects , Teicoplanin/therapeutic use , Actinomycetales Infections/microbiology , Drug Synergism , Drug Therapy, Combination , Humans , Lung Abscess/drug therapy , Lung Abscess/microbiology , Male , Middle Aged , Pneumonia, Bacterial/microbiology , Pneumonia, Bacterial/physiopathology , Severity of Illness Index , Treatment Outcome
4.
Sex Transm Infect ; 85(3): 180-1, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19478106

ABSTRACT

An ongoing outbreak of lymphogranuloma venereum (LGV) L2b proctitis, predominantly in HIV-positive men who have sex with men (MSM), has been reported in industrialised countries. A case of reactive arthritis after L2b proctitis is described. This case expands the spectrum of severe complications related to LGV L2b proctitis. Since this infection may be asymptomatic, this organism should be screened for in HIV-positive MSM with symptoms consistent with reactive arthritis.


Subject(s)
Arthritis, Reactive/etiology , Chlamydia trachomatis/isolation & purification , Homosexuality, Male , Lymphogranuloma Venereum/complications , Proctitis/complications , Adult , Chlamydia trachomatis/genetics , HIV Infections/complications , HIV-1 , Humans , Lymphogranuloma Venereum/microbiology , Male , Proctitis/microbiology
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