Literature DB >> 12010669

Chronic disseminated candidiasis in patients with hematologic malignancies. Clinical features and outcome of 29 episodes.

Livio Pagano1, Luca Mele, Luana Fianchi, Lorella Melillo, Bruno Martino, Domenico D'Antonio, Maria Elena Tosti, Brunella Posteraro, Maurizio Sanguinetti, Giulio Trapè, Francesco Equitani, Mario Carotenuto, Giuseppe Leone.   

Abstract

BACKGROUND AND OBJECTIVES: To evaluate the characteristics of patients affected by hematologic malignancies who developed a chronic disseminated candidiasis (CDC), and to ascertain the factors that influenced the outcome, in a retrospective study conducted between January 1990 and December 2000, in 4 Hematology Divisions. DESIGN AND METHODS: CDC was diagnosed by clinical features combined with radiological and/or histologic and/or microbiological data.
RESULTS: Twenty-eight patients (male/female 14/14; average age 42 years, range 12-67) developed a CDC. Twenty had acute myeloid leukemia, 5 had acute lymphocytic leukemia and 3 had non-Hodgkin's lymphoma. All patients received chemotherapy, including cytarabine for 21 of them (75%). Before the infection, 22 patients (79%) were neutropenic (absolute neutrophil count < 0.5 x 10(9)/L) for an average of 20 days (8-36), but at CDC diagnosis only 3 patients (11%) were neutropenic. Twenty-two patients (75%) received antifungal prophylaxis for an average of 15 days (10-60). Before diagnosis of CDC, 9 patients (32%) had a candidemia. The sites compromised by CDC were: liver in 27 patients (96%) and/or spleen in 11 patients (38%). Ten patients had other organs involved: lung in 6 patients (21%), kidney in 4 patients (14%), other sites 2 patients (7%). Abdominal ultrasonography was positive in 96% of patients (27/28), and abdominal computed tomography-scan was positive in 100% of cases in which it was performed (21/21). Liver biopsy was positive in 10/15 patients (67%). The main signs and symptoms were: fever 86%, abdominal pain 54%, diarrhea 32%, tenderness 25%, vomiting 25%, jaundice 29%, dysphagia 7%. Among chemical analyses, the most sensitive test was alkaline phosphatase, with a 3-5-fold increase in 24 patients (86%); an increase of liver transaminases and g-glutamyl transferase was observed in less than 50% of patients. By 30 days after diagnosis 4 patients had died, 1 from infection, and 3 progression of the hematologic malignancy without signs of active CDC. Within 3 months from diagnosis 14 out of the remaining 24 patients (58%) received further chemotherapy: in particular, 2 patients underwent transplantation procedures. INTERPRETATION AND
CONCLUSIONS: In our experience CDC is not a fatal complication of patients with hematologic malignancy, on the contrary to that observed for other fungal infections (i.e. aspergillosis, candidemia), characterized by a higher mortality rate. The major problem of this fungal complication is correlated to the delay in the following treatment for the hematologic malignancy with a high risk of progression of malignancy.

Entities:  

Mesh:

Year:  2002        PMID: 12010669

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  14 in total

1.  Caspofungin resistant disseminated candidiasis in a 7-year-old girl with T cell lymphoma: a case report.

Authors:  Michael Schmalz; Manasa Joysula; Jack H Staddon; Arthur Feinberg
Journal:  Transl Pediatr       Date:  2018-01

Review 2.  Infectious diseases and the liver.

Authors:  Rohit Talwani; Bruce L Gilliam; Charles Howell
Journal:  Clin Liver Dis       Date:  2011-02       Impact factor: 6.126

3.  Hepato-splenic candidiasis confirmed following splenectomy: a case report.

Authors:  Alexandre Peinoit; Elie Cousin; Martine Escoffre-Barbe; Marc Bernard; François Benezit; Thierry Lamy
Journal:  Infez Med       Date:  2021-12-10

4.  Successful treatment of chronic disseminated candidiasis with caspofungin and itraconazole in a patient with progressive acute leukemia and prolonged neutropenia.

Authors:  K Hübel; J Chemnitz; H G Brochhagen; O A Cornely
Journal:  Int J Hematol       Date:  2004-04       Impact factor: 2.490

5.  Epidemiology and treatment approaches in management of invasive fungal infections.

Authors:  Jane Kriengkauykiat; James I Ito; Sanjeet S Dadwal
Journal:  Clin Epidemiol       Date:  2011-05-19       Impact factor: 4.790

6.  Candidaemia in patients with haematological disorders and stem cell transplant.

Authors:  Ka Al-Anazi; Am Al-Jasser
Journal:  Libyan J Med       Date:  2006-11-21       Impact factor: 1.657

7.  Treatment of invasive fungal infections in cancer patients-updated recommendations of the Infectious Diseases Working Party (AGIHO) of the German Society of Hematology and Oncology (DGHO).

Authors:  Sabine Mousset; Dieter Buchheidt; Werner Heinz; Markus Ruhnke; Oliver A Cornely; Gerlinde Egerer; William Krüger; Hartmut Link; Silke Neumann; Helmut Ostermann; Jens Panse; Olaf Penack; Christina Rieger; Martin Schmidt-Hieber; Gerda Silling; Thomas Südhoff; Andrew J Ullmann; Hans-Heinrich Wolf; Georg Maschmeyer; Angelika Böhme
Journal:  Ann Hematol       Date:  2013-09-12       Impact factor: 3.673

8.  Chronic Disseminated Candidiasis Complicated by Immune Reconstitution Inflammatory Syndrome in Child with Acute Lymphoblastic Leukemia.

Authors:  Olga Zając-Spychała; Bogna Ukielska; Katarzyna Jończyk-Potoczna; Benigna Konatkowska; Jacek Wachowiak
Journal:  Case Rep Hematol       Date:  2016-10-09

Review 9.  Imaging of acute and subacute toxicities of cancer therapy in children.

Authors:  Govind B Chavhan; Paul S Babyn; Paul C Nathan; Sue C Kaste
Journal:  Pediatr Radiol       Date:  2015-10-12

10.  Successful management of chronic disseminated candidiasis in hematologic patients treated with high-dose liposomal amphotericin B: a retrospective study of the SEIFEM registry.

Authors:  Roberta Della Pepa; M Picardi; F Sorà; M Stamouli; A Busca; A Candoni; M Delia; R Fanci; V Perriello; M Zancanella; A Nosari; P Salutari; F Marchesi; F Pane; L Pagano
Journal:  Support Care Cancer       Date:  2016-04-14       Impact factor: 3.603

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.