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Multicentric reticulohistiocytosis: a rare cause of erosive arthropathy of the distal interphalangeal finger joints

Identifieur interne : 002201 ( Main/Exploration ); précédent : 002200; suivant : 002202

Multicentric reticulohistiocytosis: a rare cause of erosive arthropathy of the distal interphalangeal finger joints

Auteurs : D. Santilli [Italie] ; A. Lo Monaco [Italie] ; P L Cavazzini [Italie] ; F. Trotta [Italie]

Source :

RBID : ISTEX:F4C3647ACDACF88628B63F5454EAD8B7E7EB63DC

English descriptors

Abstract

Background: Multicentric reticulohistiocytosis (MRH) is a rare systemic disease, presenting with typical skin abnormalities and erosive polyarthritis, which is often associated with malignancy. Case report: A case of MRH arthropathy, in which the typical nodular skin manifestation of the disease was absent, is described in a patient with a past history of breast cancer and no evidence of recurrent or new malignancy. Results: Careful clinical and roentgenological evaluation disclosed important clues to differentiate this condition from other more common distal interphalangeal arthritides—namely, osteoarthritis and its “erosive” variant, rheumatoid arthritis, psoriatic arthritis, tophaceous gout, dialysis related hand arthropathy, and from the rarer fibroblastic rheumatism, all of which can be mimicked by MRH. Histopathology showed the characteristic histiocytic and multinucleated giant cell infiltrate with ground glass cytoplasm, and immunohistochemical analysis showed markers evocative of a monocyte/macrophage origin of MRH.

Url:
DOI: 10.1136/ard.61.6.485


Affiliations:


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Le document en format XML

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<term>MRH, multicentric reticulohistiocytosis</term>
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<term>PAS, periodic acid-Schiff</term>
<term>PsA, psoriatic arthritis</term>
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<term>Degli studi</term>
<term>Destructive arthropathy</term>
<term>Diagnostic investigation</term>
<term>Distal interphalangeal</term>
<term>Erosive</term>
<term>Erosive changes</term>
<term>Erosive polyarthritis</term>
<term>Ferrara</term>
<term>Gouty arthritis</term>
<term>Immunohistochemical analysis</term>
<term>Interphalangeal</term>
<term>Joint space</term>
<term>Malignancy</term>
<term>Methotrexate</term>
<term>Multicentric</term>
<term>Multicentric reticulohistiocytosis</term>
<term>Multinucleated</term>
<term>Multinucleated giant cells</term>
<term>Nger</term>
<term>Nger joints</term>
<term>Nodal</term>
<term>Node</term>
<term>Osteoarthritis</term>
<term>Osteoarticular disorders</term>
<term>Other hand</term>
<term>Prominent involvement</term>
<term>Psoriatic</term>
<term>Psoriatic arthritis</term>
<term>Pulse methotrexate</term>
<term>Radiological</term>
<term>Radiological evidence</term>
<term>Reticulohistiocytosis</term>
<term>Rheum</term>
<term>Rheumatoid</term>
<term>Rheumatoid arthritis</term>
<term>Rheumatol</term>
<term>Semin arthritis rheum</term>
<term>Skin nodules</term>
<term>Subchondral</term>
<term>Synovial</term>
<term>Synovial membrane</term>
<term>Tophaceous</term>
<term>Tophaceous gout</term>
<term>Trotta</term>
<term>Typical skin lesions</term>
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<div type="abstract" xml:lang="en">Background: Multicentric reticulohistiocytosis (MRH) is a rare systemic disease, presenting with typical skin abnormalities and erosive polyarthritis, which is often associated with malignancy. Case report: A case of MRH arthropathy, in which the typical nodular skin manifestation of the disease was absent, is described in a patient with a past history of breast cancer and no evidence of recurrent or new malignancy. Results: Careful clinical and roentgenological evaluation disclosed important clues to differentiate this condition from other more common distal interphalangeal arthritides—namely, osteoarthritis and its “erosive” variant, rheumatoid arthritis, psoriatic arthritis, tophaceous gout, dialysis related hand arthropathy, and from the rarer fibroblastic rheumatism, all of which can be mimicked by MRH. Histopathology showed the characteristic histiocytic and multinucleated giant cell infiltrate with ground glass cytoplasm, and immunohistochemical analysis showed markers evocative of a monocyte/macrophage origin of MRH.</div>
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