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1.
Actas Dermosifiliogr ; 115(2): T150-T158, 2024 Feb.
Article in English, Spanish | MEDLINE | ID: mdl-38048951

ABSTRACT

BACKGROUND: Dupilumab is a new targeted therapy for severe atopic dermatitis (AD) with limited real-world evidence. OBJECTIVE: Explore our experience with dupilumab for AD in clinical practice at a tertiary care center. MATERIAL AND METHOD: Unicentric observational retrospective study including adult and pediatric patients with severe AD receiving dupilumab between December 2017 and December 2021. The Eczema Area and Severity Index (EASI) score, Pruritus Numerical Rating Scale (P-NRS) and Sleep disturbance Numerical Rating Scale (S-NRS) were recovered to assess severity and response. RESULTS: Fifty-nine patients received dupilumab: 52, 48, 26 and 13 patients reached 6, 12, 24 and 36 months of treatment, respectively. The EASI-75 response rates were 94.2%, 95.8%, 92.3% and 100% at months 6, 12, 24 and 36. The EASI-90 response rates were 63.5%, 72.9%, 84.6% and 92.3% at months 6, 12, 24 and 36. The EASI <7 response rates were 92.3%, 91.7%, 88.5% and 100% at months 6, 12, 24 and 36. The P-NRS ≥4 reduction rates were 86%, 87.5%, 92.3% and 100% at months 6, 12, 24 and 36. The S-NRS ≥4 reduction rates were 82.7%, 85.4%, 100% and 100% at months 6, 12, 24 and 36. Adverse events were mild and occurred in 20.3% of patients, all of them adults. CONCLUSION: Our findings support dupilumab's favorable efficacy and tolerability profile in clinical practice. Dupilumab offers a rapid and sustained response, regardless of combined therapy. Longer follow-ups are still required to adequately assess its performance.


Subject(s)
Dermatitis, Atopic , Adult , Humans , Child , Dermatitis, Atopic/drug therapy , Retrospective Studies , Severity of Illness Index , Antibodies, Monoclonal, Humanized/adverse effects , Pruritus/chemically induced , Treatment Outcome , Double-Blind Method
2.
Actas Dermosifiliogr ; 115(2): 150-158, 2024 Feb.
Article in English, Spanish | MEDLINE | ID: mdl-37858860

ABSTRACT

BACKGROUND: Dupilumab is a new targeted therapy for severe atopic dermatitis (AD) with limited real-world evidence. OBJECTIVE: Explore our experience with dupilumab for AD in clinical practice at a tertiary care center. MATERIAL AND METHOD: Unicentric observational retrospective study including adult and pediatric patients with severe AD receiving dupilumab between December 2017 and December 2021. The Eczema Area and Severity Index (EASI) score, Pruritus Numerical Rating Scale (P-NRS) and Sleep disturbance Numerical Rating Scale (S-NRS) were recovered to assess severity and response. RESULTS: Fifty-nine patients received dupilumab: 52, 48, 26 and 13 patients reached 6, 12, 24 and 36 months of treatment, respectively. The EASI-75 response rates were 94.2%, 95.8%, 92.3% and 100% at months 6, 12, 24 and 36. The EASI-90 response rates were 63.5%, 72.9%, 84.6% and 92.3% at months 6, 12, 24 and 36. The EASI <7 response rates were 92.3%, 91.7%, 88.5% and 100% at months 6, 12, 24 and 36. The P-NRS ≥4 reduction rates were 86%, 87.5%, 92.3% and 100% at months 6, 12, 24 and 36. The S-NRS ≥4 reduction rates were 82.7%, 85.4%, 100% and 100% at months 6, 12, 24 and 36. Adverse events were mild and occurred in 20.3% of patients, all of them adults. CONCLUSION: Our findings support dupilumab's favorable efficacy and tolerability profile in clinical practice. Dupilumab offers a rapid and sustained response, regardless of combined therapy. Longer follow-ups are still required to adequately assess its performance.


Subject(s)
Dermatitis, Atopic , Adult , Child , Humans , Antibodies, Monoclonal, Humanized/adverse effects , Dermatitis, Atopic/drug therapy , Double-Blind Method , Pruritus/chemically induced , Retrospective Studies , Severity of Illness Index , Treatment Outcome
3.
Clin Exp Dermatol ; 39(4): 484-7, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24758493

ABSTRACT

Epstein-Barr virus-positive (EBV) diffuse large B-cell lymphoma (DLCBL) of the elderly is a newly described lymphoproliferative disorder that arises in elderly patients without a predisposing immunodeficiency. Clinical features at presentation may include lymphadenopathy, B-symptoms and extranodal involvement. The main sites of extranodal involvement are the skin, lung, tonsil and stomach. Histopathological findings include atypical large lymphoid cells with variable amounts of reactive cells, such as small lymphocytes, plasma cells and histiocytes. The neoplastic cells are positive for CD20, and in situ hybridization for EBV-encoded RNA is positive in the majority of neoplastic cells. We present a new case of EBV-positive DLBCL in an 85-year-old man, who presented to our clinic with a 2-month history of asymptomatic cutaneous lesions involving his face and scalp.


Subject(s)
Epstein-Barr Virus Infections/pathology , Facial Neoplasms/virology , Head and Neck Neoplasms/virology , Lymphoma, Large B-Cell, Diffuse/virology , Scalp , Skin Neoplasms/virology , Aged, 80 and over , Diagnosis, Differential , Facial Neoplasms/pathology , Head and Neck Neoplasms/pathology , Humans , Lymphoma, Large B-Cell, Diffuse/pathology , Male , Skin Neoplasms/pathology
4.
Actas Dermosifiliogr ; 105(6): 590-6, 2014.
Article in English, Spanish | MEDLINE | ID: mdl-24530124

ABSTRACT

OBJECTIVE: The aim of this study based on the records of the dermatology department of a tertiary referral hospital was to describe patients treated for allergic contact dermatitis induced by nickel between 2000 and 2010. MATERIALS AND METHODS: From records of the skin allergy section of the dermatology department we extracted and analyzed information for patients who underwent patch testing with the standard series of the Spanish Contact Dermatitis Research Group (GEIDAC), which includes a patch with 5% nickel sulfate in petroleum jelly. The possibility that nickel release from various objects might have triggered the patient's dermatitis was assessed with the dimethylglyoxime spot test, which reveals a reddish precipitate if the metal is present. RESULTS: A total of 3,404 patients underwent GEIDAC patch testing during the study period; 24.2% had positive reactions to the patch containing 5% nickel sulfate in petroleum jelly. However, the contact dermatitis could be attributed to nickel in only 57 of the 824 patients (6.9%) who showed sensitization to nickel. CONCLUSIONS: Patch-test evidence of sensitization was found to be clinically relevant in only a small percentage of patients. We emphasize the usefulness of the dimethylglyoxime test to help establish the relevance of a positive nickel patch test. This test is even useful for identifying the specific object responsible for a patient's dermatitis.


Subject(s)
Dermatitis, Allergic Contact/diagnosis , Dermatitis, Allergic Contact/etiology , Nickel/adverse effects , Adolescent , Adult , Female , Humans , Male , Middle Aged , Oximes , Patch Tests , Retrospective Studies , Tertiary Care Centers , Time Factors , Young Adult
6.
Actas Dermosifiliogr ; 101 Suppl 1: 88-96, 2010 May.
Article in Spanish | MEDLINE | ID: mdl-20492887

ABSTRACT

The introduction of tumor necrosis factor (TNF) beta blockers has make it possible to obtain a significant advance in the control and knowledge of some inflammatory diseases, among them psoriasis. TNF is a cytokine that plays a key role in the control of infections and neoplasms. The increase of the risk of developing a neoplasm during the use of this group of drugs is one of the more debated adverse effects in the literature. We present the clinical case of one patient with long-course psoriasis who developed a breast adenocarcinoma after initiating treatment with etanercept. In this article, we provide a brief review on the possible associations existing between the use of anti-TNF therapy and the risk of the appearance of come neoplasms, among which leukemias, lymphomas and some solid tumors stand out.


Subject(s)
Adenocarcinoma/chemically induced , Breast Neoplasms/chemically induced , Immunoglobulin G/adverse effects , Psoriasis/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Adult , Decision Trees , Etanercept , Female , Humans , Receptors, Tumor Necrosis Factor
7.
Actas Dermosifiliogr ; 101(8): 717-21, 2010 Oct.
Article in Spanish | MEDLINE | ID: mdl-20965015

ABSTRACT

Pyoderma gangrenosum is an inflammatory disease that has been found to be associated with many systemic illnesses. The case presented here is of a man with a 20-year history of hidradenitis suppurativa who developed pyoderma gangrenosum. The pyoderma lesions appeared as a single outbreak which resolved totally after immunosuppressive treatment. This association has been reported only rarely in the literature. Furthermore, in the cases reported, no relationship was apparent between the activity of both diseases. In all cases the clinical course appeared independent, with no apparent overlap in inflammatory activity or response to the drugs administered.


Subject(s)
Hidradenitis Suppurativa/complications , Pyoderma Gangrenosum/complications , Abscess/drug therapy , Adrenal Cortex Hormones/therapeutic use , Anti-Bacterial Agents/therapeutic use , Antibodies, Monoclonal/therapeutic use , Cyclosporine/therapeutic use , Drug Therapy, Combination , Hidradenitis Suppurativa/drug therapy , Humans , Immunosuppressive Agents/therapeutic use , Infliximab , Male , Middle Aged , Pyoderma Gangrenosum/diagnosis , Pyoderma Gangrenosum/drug therapy , Retinoids/therapeutic use , Skin Ulcer/drug therapy , Skin Ulcer/etiology , Tacrolimus/therapeutic use
8.
Actas Dermosifiliogr (Engl Ed) ; 111(3): 249-253, 2020 Apr.
Article in English, Spanish | MEDLINE | ID: mdl-31864538

ABSTRACT

BACKGROUND: The association between dipeptidyl peptidase 4 inhibitors (DPP-4i) and bullous pemphigoid (BP) has been demonstrated in several studies. The main aim of this study was to estimate the use of DPP-4i treatment in patients diagnosed with BP in our setting. METHODS: We selected patients histologically diagnosed with BP in our department between October 2015 and October 2018 and performed a retrospective chart review to assess clinical and epidemiological data and direct immunofluorescence (DIF) patterns. RESULTS: Of the 70 patients diagnosed with BP during the study period, 50% were diabetic and 88.57% of these were being treated with a DPP-4i when diagnosed with BP. The most common DPP-4i was linagliptin (used in 18.6% of patients), followed by vildagliptin (17.1%). The median latency period between initiation of DPP-4i treatment and diagnosis of BP was 27.5 months for all treatments, 16 months for linagliptin, and 39 months for vildagliptin (log rank < 0.01). A negative DIF result was significantly more common in patients not being treated with a DPP-4i. The DIF pattern most strongly (and significantly) associated with DPP-4i treatment was linear immunoglobulin G deposits along the dermal-epidermal junction. DPP-4i treatment was withdrawn in 87% of patients and 96% of these achieved a complete response. CONCLUSIONS: DPP-4i treatment is very common in patients with BP in our setting. The latency period between start of treatment and onset of BP seems to be shorter with linagliptin than with other types of gliptins. Patients receiving DPP-4i treatment may show different DIF patterns to those not receiving treatment.


Subject(s)
Dipeptidyl-Peptidase IV Inhibitors , Pemphigoid, Bullous , Dipeptidyl-Peptidase IV Inhibitors/adverse effects , Humans , Linagliptin/adverse effects , Pemphigoid, Bullous/chemically induced , Retrospective Studies , Vildagliptin
9.
Actas Dermosifiliogr (Engl Ed) ; 110(9): 728-733, 2019 Nov.
Article in English, Spanish | MEDLINE | ID: mdl-30449349

ABSTRACT

Cutaneous hemangiomas are the most frequent benign tumors in children. When they affect the lumbar and perineal area some cases can be associated with an occult spinal dysraphism. The management of these hemangiomas lack consensus. We report 3 cases of children with lumbosacral and perineal hemangiomas with magnetic resonance image abnormalities and we review the literature to find out the type and timing of tests that should be performed to complete the study in these patients. Ultrasound is typically requested as young as possible, as this imaging technique is not possible 11the posterior spinal elements have ossified. MRI is the gold standard for diagnosing occult spinal dysraphism. According to the literature, the mean age for MRI screening should be around 6 months, when the fat formation in the filum terminale is expanded. In our opinion, an MRI scan should be performed at 6 months of age in every children with lumbar or perineal hemangioma regardless the lesion size, neurological symptoms or the ultrasound results.


Subject(s)
Hemangioma/diagnostic imaging , Skin Neoplasms/diagnostic imaging , Adrenergic beta-Antagonists/therapeutic use , Female , Hemangioma/drug therapy , Humans , Infant , Lipoma/diagnostic imaging , Lumbosacral Region/diagnostic imaging , Male , Perineum/diagnostic imaging , Propranolol/therapeutic use , Skin Neoplasms/drug therapy , Spina Bifida Occulta/diagnostic imaging
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