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Neuro-radiological features can predict hypopituitarism in primary autoimmune hypophysitis.
Tartaglione, Tommaso; Chiloiro, Sabrina; Laino, Maria Elena; Giampietro, Antonella; Gaudino, Simona; Zoli, Angelo; Bianchi, Antonio; Pontecorvi, Alfredo; Colosimo, Cesare; De Marinis, Laura.
Afiliação
  • Tartaglione T; Institute of Radiology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Chiloiro S; Pituitary Unit, Department of Endocrinology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Laino ME; Institute of Radiology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Giampietro A; Pituitary Unit, Department of Endocrinology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Gaudino S; Institute of Radiology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Zoli A; Division of Rheumatology, Institute of Rheumatology and Affine Sciences, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Bianchi A; Pituitary Unit, Department of Endocrinology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Pontecorvi A; Pituitary Unit, Department of Endocrinology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • Colosimo C; Institute of Radiology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy.
  • De Marinis L; Pituitary Unit, Department of Endocrinology, School of Medicine, Catholic University of the Sacred Heart, Rome, Italy. laurademarinis@yahoo.it.
Pituitary ; 21(4): 414-424, 2018 Aug.
Article em En | MEDLINE | ID: mdl-29752700
ABSTRACT
Primary autoimmune hypophysitis (PAH) is considered an underdiagnosed disease, due to the difficulty in reaching a definitive diagnosis. PAH clinical diagnosis remains an exclusion diagnosis. We aimed to correlate PAH neuro-radiological signs to endocrine features and evaluate their prognostic role. 24 PAH cases were enrolled and classified according to neuro-radiological signs in 12 adeno-hypophysitis (AHs), 8 infundibulo-neuro-hypophysitis (INHs) and 4 pan-hypophysitis (PHs). Secondary hypogonadism developed more frequently in INHs as compared to AHs (54.5% vs. 27.3%, p = 0.05), without no difference with PHs (p = 0.6). Diabetes insipidus occurred more frequently in INHs cases (72.7%, p < 0.001) and in PHs cases (27.3%, p = 0.007), as compared to AHs cases (0%). Similarly, all cases of GHD occurred in INHs (100%) as compared to AHs (0%, p < 0.001) and PHs (0%, p < 0.001). The pituitary stalk (PS) showed a pseudo-triangular shape (larger at the optical chiasma) in INHs and a pseudo-cylindrical shape (larger both at the optical chiasma and at the pituitary insertion) in PHs. The PS pseudo-triangular shape correlated to the occurrence of GHD and diabetes insipidus (p < 0.001/p = 0.03). At the 1-year follow-up, improvement of baseline radiological features positively correlated with the loss of the neuro-pituitary "bright spot" on T1-weighted images (OR 0.16; 95% CI 0.03-0.9 p = 0.02) and with a PS diameter at the optical chiasma level larger than 4.1 mm (AUC 0.97, sensibility 80%, specificity 100%, OR 6; 95% CI1.1-28.8, p = 0.01) Our data suggest that neuro-radiological PAH classification in PH, AH and INH can predict pituitary dysfunction and that some neuro-radiological features, such as the pituitary stalk diameter and the loss of the neuro-pituitary bright spot on T1w images can play a role as a positive prognostic marker of the radiological hypophysitis outcome.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Hipófise / Hipofisite Autoimune / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças da Hipófise / Hipofisite Autoimune / Hipopituitarismo Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article