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1.
J Eur Acad Dermatol Venereol ; 34(6): 1161-1173, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31785165

ABSTRACT

Psoriatic disease is a multifaceted disorder, which develops in the skin, its appendages and joints. Though characterized by different pathogenic background and clinical manifestations, skin plaque psoriasis (PsO), psoriatic arthritis (PsA) and ankylosing spondylitis (AS) are related, sharing key inflammatory mechanisms and hence mode of management. Secukinumab is a fully human monoclonal antibody that selectively binds and neutralizes interleukin-17A. It has been approved for use as a subcutaneous injection for the treatment of moderate-to-severe PsO, PsA and AS. The current review highlights the long-term efficacy and safety profile of secukinumab in the treatment of plaque psoriasis and its multiple manifestations from its phase 3 clinical trial programme. The long-term extension of pivotal trials has shown sustainable efficacy and safety of secukinumab up to 5 years in PsO, PsA and AS and up to 2.5 years in moderate-to-severe nail and palmoplantar PsO through dedicated randomized controlled trials. The effect of secukinumab therapy in all these indications has corresponding effects on improvement in quality-of-life and daily activities. Overall, secukinumab is an effective and safe treatment choice for patients suffering from psoriatic disease in its multiple clinical variants.


Subject(s)
Arthritis, Psoriatic , Psoriasis , Antibodies, Monoclonal/adverse effects , Antibodies, Monoclonal, Humanized , Arthritis, Psoriatic/drug therapy , Humans , Psoriasis/drug therapy
3.
Clin Exp Rheumatol ; 24(2 Suppl 41): S60-4, 2006.
Article in English | MEDLINE | ID: mdl-16859598

ABSTRACT

Meningeal involvement is a rare occurrence in Wegener's Granulomatosis (WG). A Medline search uncovered only 48 previously reported cases. Here we describe the clinical features of meningeal involvement in WG and to evaluate the association with systemic disease extension. Through a systematic literature review of papers concerning meningeal involvement in WG, we collected and analysed data about sex, age, disease extension, symptoms, cerebrospinal fluid examination, imaging, ANCA and histology about previously reported patients. Headache is almost always the first symptom of meningeal involvement in WG. Later in the course of the disease other abnormalities may develop. Among them cranial nerve palsy, seizures and encephalopathy are the most frequent. Diagnosis is obtained by neuroimaging, which may disclose two distinct patterns of meningeal thickening: diffuse or focal. 62.9% of patients tests positive for ANCA. Histology typically shows necrotizing granulomatosis. Meningeal involvement is by far more frequent in the setting of localized WG. Meningitis is a rare complication of WG. It usually develops in patients with localized disease who are more likely to have destructive lesions of the upper airways. It may be recognized by a constellation of clinical and radiological findings and by histological signs of necrotizing granulomatosis, with little or no vasculitis.


Subject(s)
Granulomatosis with Polyangiitis/complications , Meninges/pathology , Meningitis/etiology , Adult , Antibodies, Antineutrophil Cytoplasmic/analysis , Cranial Nerve Diseases/etiology , Cranial Nerve Diseases/pathology , Female , Headache/etiology , Headache/pathology , Humans , Male , Meninges/chemistry , Meninges/diagnostic imaging , Meningitis/diagnosis , Meningitis/pathology , Middle Aged , Radiography , Seizures/etiology , Seizures/pathology
4.
Reumatismo ; 57(3): 187-92, 2005.
Article in Italian | MEDLINE | ID: mdl-16258603

ABSTRACT

OBJECTIVES: To evaluate the rate of different organs involvement in 50 patients with Wegener's Granulomatosis (GW), and to describe their clinical manifestations and their response to treatment. METHODS: We evaluated 50 consecutive patients with GW, come to our attention from January 1987 to May 2003. 43 patients met the 1990 American College of Rheumatology (ACR) criteria for classification of GW; 7 patients the 1993 ELK criteria. RESULTS: 82% of patients presented Ear/Nose/Throat (ENT) involvement, which is the most common site of inflammation. 22% of our patients had ENT-restricted disease; in 78% of cases disease extended to other organs. Lungs were involved in 72% of cases; kidney in 36%; eye in 24%; nervous system (NS) in 14% (central NS in 10% and peripheral NS in 4%); skin in 10%; heart in 8%; testis in 4%. Arthritis was present in 10% of patients. We discuss treatment of all patients and response to therapy of those 28 whose follow-up is available. CONCLUSIONS: Involvement of airways and kidney is by far the most common in GW, though potentially any other organ or system may be affected. The total rate of other organs involvement is 70%.


Subject(s)
Granulomatosis with Polyangiitis/complications , Adolescent , Adult , Aged , Child , Female , Granulomatosis with Polyangiitis/drug therapy , Humans , Male , Middle Aged
5.
Neurol Sci ; 26 Suppl 1: S9-14, 2005 May.
Article in English | MEDLINE | ID: mdl-15883701

ABSTRACT

Rheumatological diseases can involve the central and the peripheral nervous system in many ways. Every structure-the brain, meninges, spinal cord, cranial nerves, peripheral nerves-can be affected. Early recognition of neurological abnormality can help achieving diagnosis of the underlying condition and prevent permanent sensorimotor or cognitive function loss. This review focuses on the clinical presentation of the neurological involvement in rheumatological diseases.


Subject(s)
Nervous System Diseases/etiology , Rheumatic Diseases/physiopathology , Cognition/physiology , Connective Tissue Diseases/etiology , Humans , Rheumatic Diseases/diagnosis , Sarcoidosis/etiology , Vasculitis/etiology
7.
J Clin Microbiol ; 38(12): 4679-80, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11101624

ABSTRACT

We report the case of a 69-year-old man with acute pulmonary echinococcosis. A computed tomographic scan of the thorax revealed the presence of multiple nodules in both lungs, and laboratory tests showed eosinophilia and the presence of antibodies against Echinococcus granulosus. Therapy with albendazole led to resolution of the pulmonary nodules and a normalization of the white cell count. To our knowledge this is the first described case of acute echinococcosis, as the diagnosis of this disease is usually delayed to chronic phases. Therefore, finding unexplained eosinophilia, especially in association with pulmonary nodules, should lead one to suspect acute hydatid disease.


Subject(s)
Echinococcosis, Pulmonary/diagnosis , Acute Disease , Aged , Humans , Male
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