2016, Number 3
Pituitary involvement in granulomatosis with polyangiitis: A case report
Sandoval-Carrillo CT, Cantú-Brito C, Sandoval-Carrillo BG, Reyes MI, Díaz-Ramírez JB, Chiquete E
Language: Spanish
References: 7
Page: 113-119
PDF size: 1046.42 Kb.
ABSTRACT
Introduction: Granulomatosis with polyangiitis (formerly Wegener’s granulomatosis) is a systemic necrotizing vasculitis that usually affects the lungs and respiratory tract. The associated neurologic manifestations have been described in almost half of cases and most of them affect the peripheral nerves. The pituitary implication is uncommon.Case report: We present the case of a 50-yearold woman who met diagnostic criteria for granulomatosis with polyangiitis, having started with the classic superior and inferior respiratory condition, with pulmonary tomographic imaging that showed classic lesions in parenchyma and pleura, and a lung biopsy compatible with the diagnosis, associated with positivity to ANCA antibodies. Subsequently it was documented gastrointestinal and skin implication, with excellent response to steroid treatment. Months later the patient presented with progressive headache, polyuria and other clinical and laboratory data compatible with panhypopituitarism. By means of a head magnetic resonance it was documented involvement of the structures of the sella turcica and pituitary gland, which responded favorably to cyclophosphamide and steroids.
Conclusions: Our case of granulomatosis with polyangiitis with pituitary implication exhibited an optimal response to immunosuppressive treatment, which is consistent with what has been reported in the international literature.
REFERENCES