Juvenile Sjögren’s syndrome with a presentation of renal distal tubular acidosis

Authors

Keywords:

SJOGREN'S SYNDROME, ACIDOSIS, RENAL TUBULAR, LYMPHOCYTES, EXOCRINE GLANDS, PATIENT.

Abstract

Introduction: the Syndrome of Sjögren is an exocrinopatía autoinmune characterized by an infiltrated inflammatory, with linfocitos prevalence in glands exocrinas and knitted extraglandulares. The glandular lesion is characterized by the hiposecreción in mucous oral and ocular. 

Clinical case: a 13-year-old female adolescent with Sjögren's Syndrome is presented, whose initial clinical manifestation was extra-glandular, with the kidney as the main affected organ in type-I distal renal tubular acidosis.

Conclusions: it is demonstrated that the realization of a meticulous anamnesis, clinical exploration and the use of different diagnostic tools, they make possible a precocious diagnosis of the illness and of their manifestations extraglandulares. 

 

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Author Biographies

Didier Rodríguez Matanzas, Hospital Clínico Quirúrgico Docente León Cuervo Rubio

Especialista 1er Grado en Reumatologia

Yanet Cruz García, Hospital Clínico Quirúrgico Docente León Cuervo Rubio

Dra. Ms, Especialista en 1er Grado MGI, Especialista en 1er Grado Reumatología

References

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Published

2021-03-05

How to Cite

1.
Rodríguez Matanzas D, Cruz García Y, Urquiaga Rosa JR. Juvenile Sjögren’s syndrome with a presentation of renal distal tubular acidosis. Rev Ciencias Médicas [Internet]. 2021 Mar. 5 [cited 2025 Oct. 10];25(2):e4743. Available from: https://revcmpinar.sld.cu/index.php/publicaciones/article/view/4743

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Section

CASE REPORTS