Microscopic polyangiitis (MPA) is a rare systemic vasculitis with an incidence of about 1-3/100,000/year [1]. MPA is defined as a necrotizing vasculitis, with few or no immune deposits, primarily affecting small vessels including capillaries, venules or arterioles [2]. MPA mainly affects kidneys and lungs, nevertheless cutaneous vasculitis, musculoskeletal symptoms, gastrointestinal involvement and peripheral neuropathy also occur [3]. Circulating antineutrophil cytoplasm antibodies (ANCA) are present in about 74.5% of patients with MPA, mainly perinuclear ANCA with specificity for myeloperoxidase (p-ANCA) [4], more rarely, in about 40% of the cases, cytoplasmic ANCA with specificity to proteinase-3 (c-ANCA) are present [5]. Depending on the extent of systemic vascular involvement, clinical findings can be quite variable; nevertheless, sexual and reproductive system involvement in patients with MPA has not previously been reported.
Case reportWe report the case of a male with MPA involving the lungs, kidneys, peripheral nervous system, muscoloskeletal apparatus and the reproductive system. The patient, a 53-yearold man, was hospitalized in another institution because of malaise, slight temperature, myalgia and arthralgia, which had begun 2 months earlier; these symptoms were relieved by a steroid therapy. Systolic and diastolic blood pressure values were 130/80 mmHg, and heart rate was 75/min. Laboratory tests showed leucocytosis (WBC:11.000 U/lL) with neutrophilia (79%), microhematuria (5-10 RBC for microscopical field) and high values of erythrocite sedimentation rate (ESR 51 mm/h) and C-reactive protein (CRP 49 mg/L), whereas the remaining tests, including glycemia (86 mg/dL), total cholesterol (156 mg/dL), triglycerides (80 mg/dL) and high-density lipoprotein (52 mg/dL), were within the normal range. Moreover, c-ANCA were highly positive. The ear, throat and nose examination showed no abnormalities. A computed tomography scan of the thorax showed several opacities in the inferior pulmonary lobe, bilaterally, with no evidence of nodular or cavitary images. Seriate blood cultures, Mantoux intradermal reaction (5U reading 48 and 72 h), Widal-Wright and Weil Felix serodiagnosis as well as tumor markers were negative, thus ruling out infectious diseases and malignancies. An electroneurography revealed a bilateral peripheral neuropathy of the deep peroneal nerve as well. During hospitalization a testicular ultrasound was performed because of the onset of a dull right testicular pain. The exam depicted an enlarged right testis with a predominantly hyperechogenic area (33 mm, irregular borders), with hypoechogenic internal areas. This lesion was mainly peripherally vascularized, with poor signals internally. A smaller area with similar