Publications by authors named "Valdir S Amato"

The aim of this study was to describe a case of a patient with ocular toxoplasmosis, which has resulted in Kyrieleis plaques formation (segmental periarteritis associated with severe inflammation) and later follow-up and alternative treatment due to documented allergy to sulfonamide. A 33-year-old Brazilian woman diagnosed with acute toxoplasmosis, initially treated with sulfonamide, developed a critical cutaneous rash. Cotrimoxazole was changed to clindamycin and pyrimethamine, and prednisone was started.

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  • The study discusses the immune responses of an HIV-infected patient suffering from mucosal leishmaniasis, a condition not well understood in terms of immune reactions.
  • The patient had a notably low CD4 count of 85 cells/mm3 and experienced significant nasal damage over 2 years due to the disease.
  • Immune evaluations indicated a mixed Th1/Th2 response alongside both activated and exhausted T cells, enhancing our understanding of HIV's impact on responses to mucosal leishmaniasis.
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Background: Meglumine antimoniate (MA) remains the main treatment for cutaneous leishmaniasis (CL). Uncontrolled studies suggest that intralesional MA (IL-MA) may be noninferior and safer than systemic MA (S-MA).

Methods: Multicenter, randomized, controlled, open-label, phase 3 clinical trial to evaluate the efficacy and toxicity of IL-MA in 3 infiltrations at 14-day intervals compared with S-MA (10-20 mg Sb5+/kg/day, 20 days) for CL, with noninferiority margin of 20%.

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  • * There is a lack of investment in developing new treatments, making optimization of existing therapies via novel delivery methods, like liposomes, a viable solution.
  • * Using liposomes to encapsulate leishmanicidal drugs can enhance drug concentration in macrophages, potentially improve cure rates, reduce toxicity, and provide innovative, cost-effective treatment options.
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The immunosuppressive effect of methotrexate has rarely been associated with reactivation of cutaneous leishmaniasis. Here we present a case of a cutaneous leishmaniasis patient with atypical clinical symptoms without splenomegaly but with cutaneous manifestations after treatment of rheumatoid arthritis with methotrexate and blood recovery of the parasite. Next-generation sequencing was used to identify Leishmania infantum chagasi in the patient's blood sample.

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Human leishmaniasis is a neglected tropical disease (NTD) with high morbidity and is endemic in low- to middle-income countries. Its diagnosis, treatment and epidemiological control methods are outdated and obsolete, which has become a challenge for health practitioners in controlling the disease. Computational methods have proven to be beneficial and have become popular in many fields of medicine, especially in affluent countries.

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Leishmaniasis is a major public health problem worldwide. Although next generation sequencing technology has been widely used in the diagnosis of infectious diseases, it has been scarcely applied in identification of Leishmania species. The aim of this study was to compare the efficiency of MinION™ nanopore sequencing and polymerase chain reaction restriction fragment length polymorphism in identifying Leishmania species.

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Asymptomatic VL is a concern, considering the risk of transmission in highly endemic areas due to human-to-human transmission. The aim of this study was to report the sero-epidemiological prevalence in Bihar, India, a highly endemic area of VL, using the leishmanin skin test (LST) and the direct agglutination test (DAT). This was a cross-sectional study performed in Muzaffarpur, Bihar, India.

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Tegumentary leishmaniasis (TL) diagnosis is challenging due to the lack of a gold standard diagnostic tool. The diagnosis is significantly harder in regions where visceral leishmaniasis (VL) is also prevalent since immunological tests may present cross-reactivity. A cirrhotic patient from an endemic Brazilian region for TL and VL presented with atypical cutaneous lesions, a usual clinico-laboratory feature of VL (including a positive rk39 test result), but he was diagnosed with TL histopathologically; VL was ruled out by necropsy.

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  • Leishmaniasis is a global health issue that's often overlooked, with current treatments being inadequate.
  • A study examined the use of triglyceride-rich nanoparticles (TGNP) as a delivery method for amphotericin B (AB) to treat Leishmania amazonensis, showing better tolerability and effectiveness compared to standard AB therapy.
  • TGNP-AB demonstrated lower toxicity to healthy cells and significantly reduced the size of lesions and parasitic load in treated mice, highlighting its potential as a safer and more effective treatment option.
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  • The study investigated the effectiveness of liposomal amphotericin B (L-AMB) compared to other treatments for mucosal leishmaniasis (ML) in Brazilian patients over 15 years.
  • Results indicated that L-AMB had a higher cure rate than alternative drugs, while deoxycholate amphotericin B (d-AMB) showed greater adverse effects.
  • Despite being more effective, L-AMB was associated with acute kidney injury, highlighting the need for better therapeutic options and new drug developments for ML treatment.
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Immunosuppressive treatments for rheumatic diseases present special problems in areas endemic for chronic infectious diseases because of the possibility of reactivation. Leishmaniasis is a significant neglected tropical disease caused by different species of protozoan parasites within the genus . Amastigotes live as intracellular parasites in a variety of mammalian cells, most notably within phagocytes such as macrophages, and residual parasites can persist even after treatment and healing of the lesions.

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Rheumatoid arthritis (RA) is a chronic condition that is frequent in patients living in tropical areas exposed to leishmaniasis. RA therapy involves immunosuppressant drugs such as methotrexate (MTX), monoclonal antibodies (mAbs) and prednisone. We report an unusual presentation of cutaneous (CL) or mucocutaneous leishmaniasis (ML) in RA patients from an endemic area of leishmaniasis.

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Visceral leishmaniasis (VL) is associated with interstitial pneumonitis according to histology and radiology reports. However, studies to address the functional impact on respiratory function in patients are lacking. We assessed pulmonary function using noninvasive spirometry in a cross-sectional study of hospitalized adult VL patients from Minas Gerais, Brazil, without unrelated lung conditions or acute infections.

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  • The study aimed to determine if a less invasive blood test (kDNA-PCR) could effectively diagnose visceral leishmaniasis (VL) instead of the painful bone marrow collection (BM).
  • Researchers tested blood samples from suspected VL patients using both molecular and parasitological methods, comparing results to a combined gold standard that includes clinical evaluations and BM examinations.
  • Results showed that while kDNA-PCR in peripheral blood was highly effective in detecting VL, parasitological methods in blood were not reliable, indicating that kDNA-PCR could serve as a viable alternative to bone marrow tests.
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  • Post-kala-azar dermal leishmaniasis (PKDL) is a skin condition that can arise after treating visceral leishmaniasis (VL), primarily noted in India and Sudan but rarely reported in South America.
  • A case study details a 53-year-old Brazilian woman who developed PKDL after overcoming VL and leprosy, showing skin lesions that were confirmed to contain Leishmania parasites.
  • The findings highlight the need for careful diagnosis of PKDL, as it can closely resemble leprosy and presents challenges in distinguishing between the two conditions.
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Background/objectives: Mucosal leishmaniasis (ML) is a progressive disease that affects cartilage and bone structures of the nose and other upper respiratory tract structures. Complications associated with ML have been described, but there is a lack of studies that evaluate the structural changes of the nose and paranasal sinuses in ML using radiological methods. In this study, we aimed to assess the opacification of the paranasal sinuses in patients with treated ML and any anatomical changes in the face associated with ML using multidetector computed tomography scans (MDCT) of the sinuses.

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Background: A 36-year-old immunocompetent woman with a posterior fossa arteriovenous malformation (PF-AVM) and hydrocephalus presented with low fever and mental confusion 4 days after ventriculoperitoneal shunting (VPS).

Methods: Cerebrospinal fluid (CSF) and ventricular catheter tip cultures isolated Corynebacterium sp. Similar to previous cases in the literature, species determination was not possible.

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Mucosal leishmaniasis (ML) is a chronic form of tegumentary leishmaniasis, which causes destructive lesions of nasal, pharyngeal, and laryngeal mucosa. We describe a case of leishmaniasis reactivation with simultaneous cutaneous and mucosal forms in a renal transplanted patient with no history of prior leishmaniasis. Reactivation after renal transplantation was not reported in Brazil.

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Background: Studies assessing the efficacy of liposomal amphotericin B (LAB) in the treatment of patients with mucosal leishmaniasis (ML) are very scarce in the literature and an optimal dose regimen has not yet been defined.

Methods: We performed a retrospective and descriptive analysis from records of 16 patients with ML treated with LAB. The mean daily dose of LAB was 2.

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