Abstract

IntroductionVasculitis has been associated with malignancies, more commonly hematological rather than solid malignancies. Due to the rarity of these conditions and the lack of a temporal association, the relationship between vasculitis and malignancy remains unclear. Paraneoplastic vasculitis as a phenomenon of lung cancer has been described in the literature. To the best of our knowledge, this is the first case report of leukocytoclastic vasculitis being an initial presentation of malignant pleural mesothelioma.Case presentationWe report the case of an 84-year old Greek man who presented to our facility with an erythematous, pruritic and purpuric rash affecting his limbs. This was biopsy-proven to be leukocytoclastic vasculitis and treated conservatively with topical corticosteroids as well as oral prednisolone, with good results. Six months later, he was diagnosed as having malignant pleural mesothelioma. As he remained asymptomatic from his malignancy, no systemic chemotherapy was instituted. He had a recurrence of biopsy-proven leukocytoclastic vasculitis two months after he was diagnosed as having mesothelioma, which again settled with conservative measures.ConclusionsIt is important to remain vigilant with regard to the association between leukocytoclastic vasculitis and malignancies. A diagnosis of vasculitis requires a search for malignancies as well as other possible etiologies. This is particularly of relevance when the vasculitis becomes chronic, recurrent or treatment is no longer effective. Should our patient have experienced refractory vasculitis, we would have instituted systemic chemotherapy to treat the underlying malignancy.

Highlights

  • Vasculitis has been associated with malignancies, more commonly hematological rather than solid malignancies

  • Case presentation: We report the case of an 84-year old Greek man who presented to our facility with an erythematous, pruritic and purpuric rash affecting his limbs

  • It is important to remain vigilant with regard to the association between leukocytoclastic vasculitis and malignancies

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Summary

Conclusions

We report a case of paraneoplastic LCV as the initial presentation of MPM. To the best of our knowledge, this is the first case report of LCV presenting with MPM. Should the LCV have been steroid refractory, systemic chemotherapy was considered the option. This has not been required to date and our patient remains well without evidence of progression eight months after diagnosis. SW and TJ reviewed the manuscript and cleaned up the data. All authors reviewed and approved the final manuscript. Author details 1Austin Health, Department of Medical Oncology, 145 Studley Road, Heidelberg, Victoria 3084, Australia.

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Langford CA
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