Pustulotic arthro-osteitis complicated by polyarteritis nodosa: a case report.

Authors

Moe Asada, Masaki Matsubara, Yoshinori Uenishi, Yuki Hatta, Nobushiro Nishimura, Hiromasa Kawashima, Ryo Yoneima, Hidetoshi Matsuoka, Shiro Ono, Noritaka Yada, Hiroto Nishimura, Ryota Hara, Takayoshi Morita, Yasuhiro Akai, Kenji Nishio, Kiyomi Yoshimoto

Published in

Modern rheumatology case reports. Sep 07, 2026. Epub Sep 07, 2026.

Abstract

Pustulotic arthro-osteitis (PAO) is a chronic inflammatory disorder associated with palmoplantar pustulosis (PPP) and characterized by osteoarticular manifestations. Although several immune-mediated comorbidities have been reported in association with PPP/PAO, polyarteritis nodosa (PAN) occurring in patients with PPP/PAO has not been described previously. We report a 56-year-old woman with a long-standing history of PPP and PAO who developed worsening osteoarticular symptoms in close temporal proximity to purpura, lower-extremity pain, and sensory disturbance, followed by paresthesia in the fingers. Neurological examination revealed mild weakness of the left tibialis anterior muscle. Laboratory testing showed elevated inflammatory markers, whereas myeloperoxidase- and proteinase 3-antineutrophil cytoplasmic antibodies were negative. Musculoskeletal imaging revealed bilateral sternoclavicular joint synovitis, inflammatory changes adjacent to the right patellar tendon insertion with infrapatellar bursitis, and right peroneal tenosynovitis. Nerve conduction studies in the lower extremities suggested mononeuritis multiplex. Skin biopsy of a purpuric lesion demonstrated fibrinoid necrosis and inflammatory infiltration in medium-sized arteries within the subcutaneous tissue. The patient was diagnosed with exacerbation of PAO complicated by PAN and was treated with oral prednisolone followed by methotrexate, resulting in rapid normalization of inflammatory markers and improvement in osteoarticular symptoms, purpura, and finger paresthesia, although lower-extremity neurological symptoms persisted at discharge. When patients with PAO develop atypical features such as purpura or neuropathic symptoms suggestive of mononeuritis multiplex, concomitant vasculitis, including PAN, should be considered in the differential diagnosis.

PMID:
42704060
Bibliographic data and abstract were imported from PubMed on 07 Sep 2026.

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