Abstract

BackgroundWe report a case of a patient with a rare clinical condition: cystic angiomatosis presenting as pleural effusion and multiple bone lesions mimicking a metastatic malignant neoplasia. With only about 50 such cases published in the literature, it is important to report the clinical presentation and proposed treatment and to share information about the clinical evolution in these patients.Case presentationWe report a case of a 45-year-old white man who presented to our hospital with ventilator-dependent pain. Chest tomography detected pleural effusion and multiple osteolytic bone lesions. Oncologic investigation for metastatic malignant neoplasia was started after exclusion of an infectious process. Imaging examinations revealed diffuse osteolytic lesions as well as cystic lesions of the spleen, with discrete glycolytic hypermetabolism visualized by positron emission tomography. After negative results were obtained by investigation of the primary tumor site and a bone biopsy, a final diagnosis of cystic angiomatosis was made.ConclusionsIn view of the fact that cystic angiomatosis is a heterogeneous disorder of unpredictable prognosis and uncertain treatment, it is necessary to disseminate new cases so that further studies may be undertaken to obtain further physiopathological findings and an effective treatment.

Highlights

  • First described by Jacobs and Kimmelstiel in 1964, cystic angiomatosis is an extremely rare condition characterized by multifocal dissemination of hemangiomatous or lymphangiomatous skeletal lesions affecting the axial and appendicular skeleton, with the possible involvement of visceral organs [1, 2]

  • In view of the rarity of this clinical condition, with about 50 cases reported in the literature, we report a

  • Cystic angiomatosis is an extremely rare condition characterized by multifocal dissemination of hemangiomatous or lymphangiomatous skeletal lesions affecting the axial and appendicular skeleton, with the possible involvement of visceral organs [1, 2]

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Summary

Conclusions

In view of the fact that cystic angiomatosis is a heterogeneous disorder of unpredictable prognosis and uncertain treatment, it is necessary to disseminate new cases so that further studies may be undertaken to obtain further physiopathological findings and an effective treatment

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