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1.
Acta Derm Venereol ; 100(17): adv00284, 2020 Oct 06.
Article in English | MEDLINE | ID: mdl-32945339

ABSTRACT

Locoregional lymph node recurrences of primary trunk melanoma can occur in basins not identified during sentinel lymph node biopsy. However, the factors associated with recurrences in non-sentinel lymph node basins are unknown. To evaluate these factors, this observational retrospective study examined the patterns of first lymph node recurrence and the factors associated with recurrence in non-sentinel lymph node basins. A total of 305 patients with primary trunk melanoma who had undergone sentinel lymph node biopsy from 2000 to 2015 were evaluated. Twenty-three patients presented locoregional lymph node recurrence; 8 of which (34.8%) were in non-sentinel lymph node basins. Non-sentinel lymph node recurrences were more frequent in patients with positive sentinel lymph nodes and in those patients whose number of tumour-involved nodes was > 3. These results suggest that clinical examination and ultrasound surveillance should be performed on all potential lymph node drainage basins of trunk melanomas.


Subject(s)
Melanoma , Sentinel Lymph Node , Skin Neoplasms , Humans , Lymph Node Excision , Lymph Nodes/diagnostic imaging , Lymph Nodes/surgery , Lymphatic Metastasis , Melanoma/surgery , Neoplasm Recurrence, Local , Retrospective Studies , Sentinel Lymph Node/diagnostic imaging , Sentinel Lymph Node/surgery , Sentinel Lymph Node Biopsy , Skin Neoplasms/surgery
2.
Indian J Dermatol Venereol Leprol ; 86(5): 515-518, 2020.
Article in English | MEDLINE | ID: mdl-30688217

ABSTRACT

We report a case of a patient with Cushing's disease with oseltamivir-induced toxic epidermal necrolysis, who was treated with cyclosporine with favorable evolution. There is only one case reported of Cushing's disease and toxic epidermal necrolysis and very few oseltamivir-induced toxic epidermal necrolysis cases in literature. This report also discusses the role that the preexisting hypercortisolism condition may have played in the development and favorable resolution of the toxic epidermal necrolysis.


Subject(s)
Antiviral Agents/adverse effects , Oseltamivir/adverse effects , Pituitary ACTH Hypersecretion/diagnosis , Pituitary ACTH Hypersecretion/drug therapy , Stevens-Johnson Syndrome/diagnosis , Adult , Humans , Male , Stevens-Johnson Syndrome/therapy
3.
4.
Pediatr Dermatol ; 34(4): 465-472, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28568680

ABSTRACT

The term Mycoplasma pneumoniae-induced rash and mucositis (MIRM) was recently proposed to identify the mucocutaneous condition secondary to M. pneumoniae infection that had historically been regarded among the more confusing pathologies of erythema multiforme and Stevens-Johnson syndrome. Based on a number of previous reports, these syndromes require differentiation since they have different prognoses and specific treatment requirements. We report a case of oral and genital erosions that strongly resembled MIRM without rash but were found to be secondary to a Chlamydia pneumoniae infection. After a thorough review of the literature on this subject, we propose that C. pneumoniae should also be considered a potential causative agent of MIRM and that this term should be amended to include C. pneumoniae infection.


Subject(s)
Chlamydophila Infections/diagnosis , Mucositis/etiology , Pneumonia, Mycoplasma/diagnosis , Child , Chlamydophila , Chlamydophila Infections/complications , Diagnosis, Differential , Humans , Male , Mucositis/diagnosis , Mycoplasma pneumoniae , Pneumonia, Mycoplasma/complications
5.
J Invest Dermatol ; 137(10): 2092-2100, 2017 10.
Article in English | MEDLINE | ID: mdl-28634032

ABSTRACT

Several immunomodulatory agents are used in the treatment of epidermal necrolysis, but evidence of their efficacy is limited. The Autonomous Community of Madrid has two reference burn units to which all patients with epidermal necrolysis are referred. One burn unit has mostly used cyclosporine (CsA), and the other has used non-CsA therapies (mainly high-dose intravenous immunoglobulin). The allocation of patients to one or the other burn unit was mainly based on proximity, resembling a random assignment. Thus, we took advantage of this "natural experiment" to estimate the mortality risk ratio (MRR) of CsA (n = 26) compared with non-CsA (n = 16) treatment using hospital as an instrumental variable over the period from 2001 to 2015. We also computed the observed versus expected (O/E) MRR in a case series of 49 CsA-treated patients (including 23 patients from other regions treated in Madrid), and using the Score for Toxic Epidermal Necrolysis (i.e., SCORTEN) scale to estimate the expected values. The instrumental variable-based MRR of CsA versus non-CsA was 0.09 (95% confidence interval = 0.00-0.49). The O/E analysis also showed a reduction in mortality risk (MRROE = 0.42; 95% confidence interval = 0.14-0.99). We identified five other case series of CsA-treated patients providing MRROE and meta-analyzed their results. The pooled MRROE (including from this study) was 0.41 (95% confidence interval = 0.21-0.80). All three approaches consistently show that CsA reduces the mortality in epidermal necrolysis patients.


Subject(s)
Cyclosporine/therapeutic use , Stevens-Johnson Syndrome/drug therapy , Stevens-Johnson Syndrome/mortality , Global Health , Humans , Immunosuppressive Agents/therapeutic use , Research Design , Survival Rate/trends
6.
Pharmacol Res ; 115: 168-178, 2017 01.
Article in English | MEDLINE | ID: mdl-27888155

ABSTRACT

Aromatic antiepileptic drugs (AEDs) are among the drugs most frequently involved in severe cutaneous adverse reactions (SCARs), such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reactions with eosinophilia and systemic symptoms (DRESS). This study investigated the associations between the genetic polymorphisms of HLA class-I and AED-induced SCARs in the Spanish population. HLA class-I genotypes were determined in AED (phenytoin[PHT],lamotrigine[LTG],carbamazepine[CBZ],phenobarbital[PB])-induced SJS/TEN (n=15) or DRESS (n=12) cases included in the Spanish SCAR registry, PIELenRed. There were 3 control groups: (A)tolerant to a single AED, (B)tolerant to any AED, and (C)Spanish population controls. For SJS/TEN, concomitant HLA-A*02:01/Cw15:02 alleles were significantly associated with PHT-cases compared to control groups B and C [(B)odds ratio(OR):14.75, p=0.009;(C)OR:27.50, p<0.001], and were close to significance with respect to control group A (p=0.060). The genotype frequency of the HLA-B*38:01 was significantly associated with PHT-LTG-cases compared with the 3 groups of controls [(A)OR:12.86, p=0.012;(B)OR:13.81; p=0.002;(C)OR:14.35, p<0.001], and with LTG-cases [(A)OR:147.00, p=0.001;(B)OR:115.00, p<0.001;(C)OR:124.70, p<0.001]. We found the HLA-B*15:02 allele in a Spanish Romani patient with a CBZ-case. The HLA-A*11:01 was significantly associated with CBZ-cases [(A)OR:63.89, p=0.002;(B)OR:36.33, p=0.005;(C)OR:28.29, p=0.007]. For DRESS, the HLA-A*24:02 genotype frequency was statistically significant in the PHT-LTG-cases [(A)OR:22.56, p=0.003;(B)OR:23.50. p=0.001; (C)OR:33.25, p<0.001], and in the LTG-cases [(A),OR:49.00, p=0.015;(B)OR:27.77, p=0.005; (C)OR:34.53, p=0.002]. HLA-A*31:01 was significantly associated with the CBZ-cases [(A)OR:22.00, p=0.047;(B)OR:29.50, p=0.033;(C)OR:35.14, p=0.006]. In conclusion, we identified several significant genetic risk factors for the first time in the Spanish Caucasian population: HLA-A*02:01/Cw*15:02 combination as a risk factor for PHT-induced SJS/TEN, HLA-B*38:01 for LTG- and PHT- induced SJS/TEN, HLA-A*11:01 for CBZ-induced SJS/TEN, and HLA-A*24:02 for LTG- and PHT- induced DRESS. The strong association between HLA*31:01 and CBZ-DRESS in Europeans was confirmed in this study.


Subject(s)
Anticonvulsants/adverse effects , Drug Hypersensitivity Syndrome/genetics , Genes, MHC Class I/genetics , Genetic Predisposition to Disease/genetics , Stevens-Johnson Syndrome/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Drug Hypersensitivity Syndrome/etiology , Female , Genotype , Humans , Male , Middle Aged , Polymorphism, Genetic , Risk Factors , Spain , Stevens-Johnson Syndrome/etiology , White People/genetics , Young Adult
7.
Br J Clin Pharmacol ; 83(2): 400-415, 2017 02.
Article in English | MEDLINE | ID: mdl-27543764

ABSTRACT

AIM: We conducted a prospective evaluation of all eosinophilic drug reactions (EDRs) through the Prospective Pharmacovigilance Program from Laboratory Signals at Hospital to find out the incidence and distribution of these entities in our hospital, their causative drugs, and predictors. METHODS: All peripheral eosinophilia >700 × 106  cells l-1 detected at admission or during hospitalisation, were prospectively monitored over 42 months. The spectrum of the localised or systemic manifestation of EDR, the incidence, the distribution of causative drugs, and the predictors were analysed. RESULTS: The incidence of EDR was 16.67 (95% Poisson confidence interval [CI]: 9.90-25.98) per 10 000 admissions. Of 274 cases of EDR, 154 (56.2%) cases in 148 patients were asymptomatic hypereosinophilia. In the remaining 120 (43.8%) cases, there was other involvement. Skin and soft tissue reactions were detected in 36 (13.1%) cases; visceral EDRs in 19(7.0%) cases; and drug-induced eosinophilic cutaneous and visceral manifestations were detected in the remaining 65 (23.7%) cases, 64 of which were potential drug reaction with eosinophilia and systemic symptoms (DRESS). After adjusting for age, sex, and hospitalisation wards, predictors of symptomatic eosinophilia were earlier onset of eosinophilia (hazard ratio [HR], 10.49; 95%CI: 3.13-35.16) higher eosinophil count (HR, 8.51; 95%CI: 3.28-22.08), and a delayed onset of corticosteroids (HR, 1.34; 95%CI: 1.01-1.73). A higher eosinophil count in patients with DRESS was significantly associated with greater impairment of liver function, prolonged hospitalisation, higher cumulative doses of corticosteroids, and if hypogammaglobinaemia was detected, a reactivation of human-herpesvirus 6 was subsequently detected. CONCLUSIONS: Half (53.3%, 64/120 cases) of symptomatic EDRs were potential DRESS. The main predictor of severity of EDR was an early severe eosinophilia.


Subject(s)
Drug Hypersensitivity Syndrome/epidemiology , Drug-Related Side Effects and Adverse Reactions/epidemiology , Eosinophilia/chemically induced , Pharmacovigilance , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Drug Eruptions/epidemiology , Drug Eruptions/etiology , Drug Eruptions/pathology , Drug Hypersensitivity Syndrome/etiology , Drug Hypersensitivity Syndrome/physiopathology , Eosinophilia/epidemiology , Eosinophilia/physiopathology , Female , Hospitalization , Humans , Incidence , Infant , Male , Middle Aged , Prospective Studies , Severity of Illness Index , Tertiary Care Centers , Young Adult
8.
Dermatol Ther ; 29(1): 32-6, 2016.
Article in English | MEDLINE | ID: mdl-26445325

ABSTRACT

Pachyonychia congenita (PC) is a rare genodermatosis caused by a mutation in keratin genes, which can lead to hypertrophic nail dystrophy and focal palmoplantar keratoderma (predominantly plantar), amongst other manifestations. Painful blisters and callosities, sometimes exacerbated by hyperhidrosis, are major issues that can have a significant impact on patient quality of life. Many alternative treatments for this condition have been applied with variable and partial clinical response, but a definitive cure for this disease has yet to be discovered. After obtaining informed consent, two patients with genetically confirmed PC type 1 were treated with plantar injections of botulinum toxin type A. Both patients showed a marked improvement in pain and blistering with an average response time of one week, a six-month mean duration of effectiveness, and a lack of any side effects or tachyphylaxis.


Subject(s)
Botulinum Toxins, Type A/administration & dosage , Foot Dermatoses/drug therapy , Keratoderma, Palmoplantar/drug therapy , Nails, Malformed/drug therapy , Pachyonychia Congenita/drug therapy , Skin/drug effects , Adult , DNA Mutational Analysis , Female , Foot Dermatoses/genetics , Foot Dermatoses/pathology , Genetic Predisposition to Disease , Humans , Injections, Intradermal , Keratin-6/genetics , Keratoderma, Palmoplantar/genetics , Keratoderma, Palmoplantar/pathology , Male , Mutation, Missense , Nails, Malformed/genetics , Nails, Malformed/pathology , Pachyonychia Congenita/genetics , Pachyonychia Congenita/pathology , Phenotype , Remission Induction , Skin/pathology , Time Factors , Treatment Outcome
9.
Indian J Dermatol ; 60(4): 423, 2015.
Article in English | MEDLINE | ID: mdl-26288449

ABSTRACT

Cirsoid aneurysm is a small vascular proliferation characterized by small to medium-sized channels with features of arteries and veins, that present as small, blue or red asymptomatic papule. We report a case of a crisoid aneurysm on the forhead of an HIV patient that suggested a Kaposi sarcoma as a differential diagnosis.

11.
Am J Dermatopathol ; 37(7): 581-4, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25140665

ABSTRACT

Diffuse dermal angiomatosis is a rare benign condition considered a variant of reactive angioendotheliomatosis, usually related to vascular disease such as arteriovenous fistula or severe peripheral vascular disease. The most frequent clinical manifestations range from a solitary erythematous patch to an indurated plaque that may ulcerate. A clinical case of a 60-year-old woman who developed generalized livedoid lesions 2 days after the administration of intravenous trabectedin and subcutaneous pegfilgrastim for a recidivant myxoid liposarcoma has been reported. A biopsy of the skin lesions showed a pronounced proliferation of vessels in the upper dermis that was diagnosed as diffuse dermal angiomatosis.


Subject(s)
Angiomatosis/chemically induced , Drug Eruptions/etiology , Endothelial Cells/drug effects , Skin Diseases, Vascular/chemically induced , Angiomatosis/pathology , Antigens, CD34/analysis , Antineoplastic Agents, Alkylating/adverse effects , Cell Proliferation , Dioxoles/adverse effects , Drug Eruptions/pathology , Endothelial Cells/chemistry , Endothelial Cells/pathology , Female , Filgrastim , Granulocyte Colony-Stimulating Factor/adverse effects , Humans , Middle Aged , Platelet Endothelial Cell Adhesion Molecule-1/analysis , Polyethylene Glycols , Recombinant Proteins/adverse effects , Skin Diseases, Vascular/pathology , Tetrahydroisoquinolines/adverse effects , Trabectedin
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