POLYARTERITIS NODOSA MANIFESTING AS PARANEOPLASTIC SYNDROME

POLYARTERITIS NODOSA MANIFESTING AS PARANEOPLASTIC SYNDROME

MELO, ELISA FERNANDES DE; SOUBIHE, VINICIUS VERLANGIERI; ANATE, RAYLANE SHELLYDA DE ALMEIDA; RAVASIO, NATÁLIA ENGLER; JUNIOR, AMAURI MARCELO CISOTTO ROCHA; ESTEVAM, PAULO GIOVANNI; ESTEVES, LARISSA ALMEIDA CAMPOS; PAVANITTO, DRIELLE REZENDE; GUERRA, ALINE GIMENEZ

Pôster:

Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis with a predilection for the arteries of medium and small caliber. The diagnosis of any vasculitis should be carried out in a judicious manner, always resorting to the possibility of differential diagnoses. Even when confirmed, there is the possibility of being secondary to neoplasms, infections and drug exposures. The pathogenesis of paraneoplastic syndrome is due to secretions of substances such as hormones or immune-mediated mechanisms. They may appear before, after or concomitantly with the neoplasm, but about 71% of the cases occur before tumor discovery or during recurrence. Due to the rareness of the association between PAN and paraneoplastic syndrome and because it is related to a worse prognosis, the occurrence of this association should be reported.

Case report

A 43-year-old woman, smoker (20 pack-years) reported Raynaud's phenomenon for 4 years, evolving to livedo reticularis in the past 6 months associated with weight loss of 6 Kg and lack of appetite. In the last 2 months presented painful blisters and cyanotic lesions at extremities (figure 1) and a sudden reduction of visual acuity. Central venous occlusion of the retina was observed bilaterally in the ophthalmologic evaluation. It evolved with worsening and ascendant and loss of peripherical pulses. Complete blood count showed chronic disease’s anemia, leukocytosis, increased inflammatory tests and normal renal function. Performed ANCA, ANA, anti-Ro, anti-CCP, serology for HIV, hepatitis B and C all with negative results. Initiated antibiotic therapy, anticoagulation, pulse therapy with cyclophosphamide and methylprednisolone, and immunoglobulin. An attempt was made for surgical debridement, evolving with mummification of the forearm and legs, and due to the infeasibility, amputation was chosen. A biopsy showed septal panniculitis associated with arteritis in medium-caliber vessels. Due to the refractoriness of the immunosuppressive treatment, the hypothesis of polyarteritis nodosa secondary to paraneoplastic syndrome was proposed. Investigation of the primary site was started, with probable pulmonary focus, however after 45 days of hospitalization, the patient died.

Conclusion

PAN is a vasculitis with clinical diagnostic criteria, according to the American College of Rheumatology, but whenever possible, it should be confirmed by biopsy. If not treated, it is usually lethal. In addition, the lack of clinical response to treatment may be an alert to think of a secondary cause, such as paraneoplastic.

Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis with a predilection for the arteries of medium and small caliber. The diagnosis of any vasculitis should be carried out in a judicious manner, always resorting to the possibility of differential diagnoses. Even when confirmed, there is the possibility of being secondary to neoplasms, infections and drug exposures. The pathogenesis of paraneoplastic syndrome is due to secretions of substances such as hormones or immune-mediated mechanisms. They may appear before, after or concomitantly with the neoplasm, but about 71% of the cases occur before tumor discovery or during recurrence. Due to the rareness of the association between PAN and paraneoplastic syndrome and because it is related to a worse prognosis, the occurrence of this association should be reported.

Case report

A 43-year-old woman, smoker (20 pack-years) reported Raynaud's phenomenon for 4 years, evolving to livedo reticularis in the past 6 months associated with weight loss of 6 Kg and lack of appetite. In the last 2 months presented painful blisters and cyanotic lesions at extremities (figure 1) and a sudden reduction of visual acuity. Central venous occlusion of the retina was observed bilaterally in the ophthalmologic evaluation. It evolved with worsening and ascendant and loss of peripherical pulses. Complete blood count showed chronic disease’s anemia, leukocytosis, increased inflammatory tests and normal renal function. Performed ANCA, ANA, anti-Ro, anti-CCP, serology for HIV, hepatitis B and C all with negative results. Initiated antibiotic therapy, anticoagulation, pulse therapy with cyclophosphamide and methylprednisolone, and immunoglobulin. An attempt was made for surgical debridement, evolving with mummification of the forearm and legs, and due to the infeasibility, amputation was chosen. A biopsy showed septal panniculitis associated with arteritis in medium-caliber vessels. Due to the refractoriness of the immunosuppressive treatment, the hypothesis of polyarteritis nodosa secondary to paraneoplastic syndrome was proposed. Investigation of the primary site was started, with probable pulmonary focus, however after 45 days of hospitalization, the patient died.

Conclusion

PAN is a vasculitis with clinical diagnostic criteria, according to the American College of Rheumatology, but whenever possible, it should be confirmed by biopsy. If not treated, it is usually lethal. In addition, the lack of clinical response to treatment may be an alert to think of a secondary cause, such as paraneoplastic.

Palavras-chave:

DOI: 10.5151/sbr2019-206

Referências bibliográficas

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Como citar:

MELO, ELISA FERNANDES DE; SOUBIHE, VINICIUS VERLANGIERI; ANATE, RAYLANE SHELLYDA DE ALMEIDA; RAVASIO, NATÁLIA ENGLER; JUNIOR, AMAURI MARCELO CISOTTO ROCHA; ESTEVAM, PAULO GIOVANNI; ESTEVES, LARISSA ALMEIDA CAMPOS; PAVANITTO, DRIELLE REZENDE; GUERRA, ALINE GIMENEZ; "POLYARTERITIS NODOSA MANIFESTING AS PARANEOPLASTIC SYNDROME", p-206-206. In: Anais do 36º Congresso Brasileiro de Reumatologia. [ISBN 978-85-212-1892-0]. São Paulo: Blucher, 2019.
ISSN 23577282, DOI 10.5151/sbr2019-206