Vasculite cutanéo-systémique révélant un carcinome papillaire thyroïdien

Boyé, T.; Gisserot, O.; Guennoc, B.; Thouard, P.; Carsuzaa, F.

doi:10.1016/s0248-8663(00)90315-1

Cited by 2 publications

(3 citation statements)

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“…The histological type of the thyroid cancer was not mentioned in these latter two cases. Apart from the case of Boye et al ., which was identical to our patient, no systemic disorder was reported in any of these patients, but total thyroidectomy resulted in complete healing in all of them, as in our patient.…”

Section: Reportsupporting

confidence: 77%

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Systemic paraneoplastic vasculitis secondary to papillary carcinoma of the thyroid

et al. 2016

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Systemic vasculitis secondary to thyroid carcinomas is exceptional. We report the case of a 55-year-old woman who presented with systemic vasculitis involving leucocytoclastic cutaneous vasculitis and renal disorders secondary to papillary thyroid carcinoma (PTC). Her symptoms resolved completely after total thyroidectomy. Other causes of vasculitis were excluded. To our knowledge, this is only the second case reported of systemic vasculitis associated with PTC in a paraneoplastic manner.

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Section: Reportsupporting

confidence: 77%

“…Paraneoplastic vasculitis secondary to PTC is exceptional. Our examination of the existing literature identified only one identical case of systemic vasculitis secondary to PTC, involving CLV and urinary disorders (haematuria and proteinuria) in a 51‐year‐old man . Pierru et al .…”

Section: Reportmentioning

confidence: 97%

Systemic paraneoplastic vasculitis secondary to papillary carcinoma of the thyroid

et al. 2016

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“…On the other hand, other interesting cases connect rheumatology and endocrinology. We used the database PubMed and studied a total of ten cases that included patients with rheumatological diseases and papillary carcinoma of the thyroid gland (see table) (4)(5)(6)(7)(8)(9)(10)(11)(12)(13). The cases consisted of three men and seven women aged 31 to 69 years and tumour sizes from 19 to 40 mm.…”

Section: Discussionmentioning

confidence: 99%

Association of Giant Cell Arteritis with Papillary Thyroid Carcinoma

Šípová

Havlínová

Bělobrádková

et al. 2022

Acta Med. (Hradec Kralove, Czech Repub.)

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Previous studies suggest that there may be an association between cancer and autoimmune diseases. We describe the case of a 59-year-old patient who did not have any significant diseases in the last year. She had new onset of fever of unknown aetiology, headache, fatigue and night sweats. We used laboratory methods to rule out infectious diseases. Significant laboratory findings reported increased signs of inflammation and anti-nuclear antibody (ANA) positivity. Positron emission tomography/computed tomography (PET/CT) imaging showed the origin of the patient’s difficulties, arteritis, with increased metabolic activity in the aortic wall and other arteries. Doppler ultrasonography of the arteries did not show pathology in the temporal arteries but found accelerated blood flow in the superior mesenteric artery (AMS). Another finding from PET/CT was a tumour in the thyroid gland, later verified histologically as papillary thyroid carcinoma (PTC). We investigated the link between rheumatological disease and papillary carcinoma, applying similar therapy, corticosteroids and immunosuppressants.

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Vasculite cutanéo-systémique révélant un carcinome papillaire thyroïdien

Cited by 2 publications

References 0 publications

Systemic paraneoplastic vasculitis secondary to papillary carcinoma of the thyroid

Systemic paraneoplastic vasculitis secondary to papillary carcinoma of the thyroid

Association of Giant Cell Arteritis with Papillary Thyroid Carcinoma

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