Latin American Clinical Practice Guidelines on the Systemic Treatment of PsoriasisSOLAPSO– Sociedad Latinoamericana de Psoriasis(Latin American Psoriasis Society)

2019 ◽  
Vol 58 (S1) ◽  
pp. 4-28 ◽  
Author(s):  
Nora Kogan ◽  
Nélida Raimondo ◽  
Simon E. Gusis ◽  
Ariel Izcovich ◽  
Jorge A. Abarca Duran ◽  
...  
Breast Cancer ◽  
2020 ◽  
Vol 27 (3) ◽  
pp. 322-331 ◽  
Author(s):  
Tatsunori Shimoi ◽  
Shigenori E. Nagai ◽  
Tetsuhiro Yoshinami ◽  
Masato Takahashi ◽  
Hitoshi Arioka ◽  
...  

2019 ◽  
Vol 48 (2) ◽  
pp. 030006051986354 ◽  
Author(s):  
Héctor Cruz-Camino ◽  
Diana Laura Vazquez-Cantu ◽  
Alexandra Vanessa Zea-Rey ◽  
Jaime López-Valdez ◽  
Jorge Jiménez-Lozano ◽  
...  

Hawkinsinuria is an autosomal dominant disorder of tyrosine metabolism. Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene ( HPD) result in an altered HPD enzyme, causing hawkinsin and tyrosine accumulation. Persistent metabolic acidosis and failure to thrive are common features in patients with hawkinsinuria. We present the first known Latin American patient diagnosed with hawkinsinuria, and the tenth reported patient in the literature. We aim to establish clinical practice guidelines for patients with hawkinsinuria. The patient’s plasma tyrosine level was 21.5 mg/dL, which is several times higher than the reference value. Mutation analysis indicated heterozygosity for V212M and A33T variants in HPD. In the case of altered tyrosine levels found during newborn screening, we propose exclusive breastmilk feeding supplemented with ascorbic acid. Amino acid quantification is useful for monitoring treatment response. If tyrosinemia persists, protein intake must be decreased via a low-tyrosine diet. Molecular studies can be used to confirm a patient’s disease etiology. Further reports are required to elucidate new pathogenic and phenotypic variations to enable the development of an appropriate therapeutic approach.


2014 ◽  
Vol 13 ◽  
pp. S4-S40 ◽  
Author(s):  
Nahum Méndez-Sánchez ◽  
Ezequiel Ridruejo ◽  
Angelo Alves de Mattos ◽  
Norberto C. Chávez-Tapia ◽  
Rodrigo Zapata ◽  
...  

Breast Cancer ◽  
2021 ◽  
Author(s):  
Tatsunori Shimoi ◽  
Shigenori E. Nagai ◽  
Tetsuhiro Yoshinami ◽  
Masato Takahashi ◽  
Hitoshi Arioka ◽  
...  

A correction to this paper has been published: https://doi.org/10.1007/s12282-021-01252-x


2019 ◽  
Vol 18 (3) ◽  
pp. 518-535 ◽  
Author(s):  
Juan P. Arab ◽  
Juan P. Roblero ◽  
Jose Altamirano ◽  
Fernando Bessone ◽  
Roberta Chaves Araujo ◽  
...  

2018 ◽  
Vol 77 (11) ◽  
pp. 1549-1557 ◽  
Author(s):  
Bernardo A Pons-Estel ◽  
Eloisa Bonfa ◽  
Enrique R Soriano ◽  
Mario H Cardiel ◽  
Ariel Izcovich ◽  
...  

Systemic lupus erythematosus (SLE), a complex and heterogeneous autoimmune disease, represents a significant challenge for both diagnosis and treatment. Patients with SLE in Latin America face special problems that should be considered when therapeutic guidelines are developed. The objective of the study is to develop clinical practice guidelines for Latin American patients with lupus. Two independent teams (rheumatologists with experience in lupus management and methodologists) had an initial meeting in Panama City, Panama, in April 2016. They selected a list of questions for the clinical problems most commonly seen in Latin American patients with SLE. These were addressed with the best available evidence and summarised in a standardised format following the Grading of Recommendations Assessment, Development and Evaluation approach. All preliminary findings were discussed in a second face-to-face meeting in Washington, DC, in November 2016. As a result, nine organ/system sections are presented with the main findings; an ‘overarching’ treatment approach was added. Special emphasis was made on regional implementation issues. Best pharmacologic options were examined for musculoskeletal, mucocutaneous, kidney, cardiac, pulmonary, neuropsychiatric, haematological manifestations and the antiphospholipid syndrome. The roles of main therapeutic options (ie, glucocorticoids, antimalarials, immunosuppressant agents, therapeutic plasma exchange, belimumab, rituximab, abatacept, low-dose aspirin and anticoagulants) were summarised in each section. In all cases, benefits and harms, certainty of the evidence, values and preferences, feasibility, acceptability and equity issues were considered to produce a recommendation with special focus on ethnic and socioeconomic aspects. Guidelines for Latin American patients with lupus have been developed and could be used in similar settings.


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