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Dive into the research topics where Emmilia Hodak is active.

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Featured researches published by Emmilia Hodak.


British Journal of Dermatology | 2006

Mycosis fungoides associated with B-cell malignancies

A. Barzilai; H. Trau; Michael David; Meora Feinmesser; R. Bergman; D. Shpiro; G. Schiby; K. Rosenblatt; R. Or; Emmilia Hodak

Backgroundu2002 The coexistence of mycosis fungoides, a peripheral T‐cell lymphoma, and B‐cell malignancies or Hodgkins lymphoma in the same patient is unusual. Most descriptions are isolated case reports and case series are strikingly sparse.


Journal of The American Academy of Dermatology | 2003

Climatotherapy at the Dead Sea is a remittive therapy for psoriasis: combined effects on epidermal and immunologic activation

Emmilia Hodak; Alice B. Gottlieb; Tsvi Segal; Yael Politi; Lea Maron; Jaqueline Sulkes; Michael David

BACKGROUNDnThe beneficial effect of climatotherapy at the Dead Sea (CDS) for psoriasis has been established clinically but there is a striking lack of studies assessing its in vivo effect at the molecular and cellular levels.nnnOBJECTIVEnWe sought to study the response of activated immunologic cells and keratinocytes in psoriatic lesions to CDS.nnnMETHODSnA total of 27 patients with chronic, stable, plaque-type psoriasis treated with CDS for 28 consecutive days were evaluated with the Psoriasis Area and Severity Index score and quantitative histologic measures.nnnRESULTSnAfter 4 weeks of treatment, the overall Psoriasis Area and Severity Index score decreased by 81.5%. Complete clearance was achieved in 48% of the patients, and moderate to marked improvement in 41%. The average duration of remission was 3.3 months. Histologically, there was an overall reduction in malpighian layer thickness by 63.4%, and keratinocyte hyperplasia, assessed by Ki-67 cell cycle antigen expression, decreased by 78%; residual cell proliferation was confined mainly to the basal layer. These changes were accompanied by normalization of keratin 16 expression in 90% of the patients. T lymphocytes were almost totally eliminated from the epidermis (depletion of >90% of CD3(+) and CD25(+) cells), with only a low number remaining in the dermis (depletion of 69.4% of CD3(+) cells and 77.4% of CD25(+) cells). This reduction in activated T cells was accompanied by a marked reduction in HLA-DR expression by epidermal keratinocytes.nnnCONCLUSIONSnCDS is a highly effective and remittive treatment for moderate to severe plaque-type psoriasis, leading to a reversal of both pathologic epidermal and immunologic activation.


British Journal of Dermatology | 1997

Lupus miliaris disseminatus faciei—the DNA of Mycobacterium tuberculosis is not detectable in active lesions by polymerase chain reaction

Emmilia Hodak; Akiva Trattner; H. Feuerman; Meora Feinmesser; R. Tsvieli; S. Mitrani-Rosenbaum; Michael David

There has been a controversy as to the origin of lupus miliaris disseminatus faciei (LMDF). It was originally thought to be associated with tuberculosis, due to its histopathological similarity. Recently, this association has been doubted, although there remain reported cases of LMDF associated with Mycobacterium tuberculosis. Three patients with the clinical and histopathological features of LMDF are described. Skin from these patients was analysed by polymerase chain reaction (PCR) using two different oligoprimers for the detection of 123 bp and 165 bp DNA fragments specific for M. tuberculosis complex. With these two PCR systems, no M. tuberculosis DNA was detected in any of the LMDF patients. It was present in all positive controls and absent in all negative controls. In this study we could not demonstrate an association between LMDF and tuberculosis.


British Journal of Dermatology | 2001

Mycosis fungoides: HLA class II associations among Ashkenazi and non-Ashkenazi Jewish patients

Emmilia Hodak; M. Lapidoth; Y. Kohn; Michael David; C. Brautbar; B. Kfir; R. Narinski; C. Safirman; L. Maron; Tirza Klein

Backgroundu2003An immunogenetic mechanism has been suggested to play a role in the pathogenesis of mycosis fungoides (MF). While results of studies on HLA class I associations have proved inconsistent, two previous studies showed that certain HLA class II alleles were significantly increased among North American caucasian patients with MF: HLA‐DRB1*11 and DQB1*03.


Journal of The American Academy of Dermatology | 1999

Effect of colchicine in the subcorneal pustular dermatosis type of IgA pemphigus

Emmilia Hodak; Moshe Lapidoth; Michael David

BACKGROUNDnIgA pemphigus of the subcorneal pustular dermatosis (SPD) type is characterized by subcorneal acantholysis and by an abundance of neutrophils, making colchicine a reasonable pharmacologic option for treatment.nnnOBJECTIVEnWe attempted to determine the efficacy of colchicine in the treatment of SPD-type IgA pemphigus.nnnMETHODSnTwo patients with SPD-type IgA pemphigus were treated with colchicine 1.5 mg/day as monotherapy.nnnRESULTSnA sustained clinical response was achieved within 2 to 3 weeks of therapy. Relapses were noted each time colchicine was stopped.nnnCONCLUSIONnColchicine should be considered in the treatment of SPD-type IgA pemphigus.


Annals of Pharmacotherapy | 1990

Fixed Drug Eruption following Rifampin Treatment

Aviva Mimouni; Emmilia Hodak; Marc Mimouni

A case of fixed drug eruption (FDE) associated with ingestion of rifampin in a young physician is reported. The drug was prophylactically administered because of a previous close contact with a meningococcemic patient. The eruption consisted of two solitary painless purplish lesions located over the extensor surface of the left forearm, characteristic of FDE, except for the absence of residual hyperpigmentation. It is suggested that slight lesions of FDE could be unnoticed or misdiagnosed, thus raising the possibility that such skin reactions to rifampin are more frequent than is reflected in the literature.


International Journal of Dermatology | 2006

Early-stage mycosis fungoides, parapsoriasis en plaque, and pregnancy.

Iris Amitay-Layish; Michael David; Batia Kafri; Aviv Barzilai; Meora Feinmesser; Emmilia Hodak

Backgroundu2002 Non‐Hodgkins lymphoma (NHL) coincident with pregnancy is rare, and the literature regarding mycosis fungoides (MF), the most common primary cutaneous NHL, and pregnancy is strikingly sparse. The effect of pregnancy on MF, or on parapsoriasis en plaque (PPP), and the effect of these diseases on pregnancy, are still unknown.


Journal of Cutaneous Pathology | 1996

In vivo expression of the insulin-like growth factor-I (IGF-I) receptor in congenital pigmented nevi

Emmilia Hodak; Alice B. Gottlieb; S. Colen; M. Anzilotti; James G. Krueger

Growth of normal melanocytes, nevus cells and primary melanoma cells is enhanced by insulin/insulin‐like growth factor‐I (IGF‐I) in vitro. It has been shown that a melanoma cell line possesses the IGF‐I receptor which plays a role in activation of the chemotactic response. Little is known about the in vivo expression of the IGF‐I receptor and its role in melanocytic lesions. In an immunohistochemical study, we investigated the expression of IGF‐I receptor in frozen sections of congenital pigmented nevi from 10 patients (ages 8 months to 4 yrs) using the monoclonal antibody αIR3, which specifically recognizes the extracellular alpha subunit of the IGF‐I receptor. The proliferative activity of the nevus cells was examined by staining with Ki67 monoclonal antibody (reactive with all actively cycling cells). IGF‐I receptor was found to be widely expressed by the cell surface of the nevus cells. Membrane staining was occasionally stronger in the superficial portion of the congenital pigmented nevi. In contrast, Ki67‐positive cells were only sparsely scattered throughout the nevi with some tendency to localization to the superficial portion.


Acta Dermato-venereologica | 2005

Cytokine gene polymorphisms in patch-stage mycosis fungoides.

Emmilia Hodak; Lehavit Akerman; Michael David; Anat R. Tambur; Batia Kfir; Leah Maron; Jacqueline Sulkes; Tirza Klein

Cytokine production is under genetic control and certain allelic variants of cytokine genes are associated with lower or higher cytokine production in vitro and in vivo. The general concept is that a shift from a Th1 to a Th2 cytokine profile accompanies disease progression from patch-stage mycosis fungoides to tumour stage, although the results of the studies carried out have not been entirely conclusive. We aimed to investigate whether certain cytokine polymorphisms might represent a risk factor for developing patch-stage mycosis fungoides. Genotyping for IFN-gamma (Th1 cytokine), IL-6, IL-10 (Th2 cytokines), TNF-alpha and TGF-beta 1 was undertaken for 33 patients with patch-stage mycosis fungoides and the results were compared with those in a control group. Genotype distribution showed no significant differences between the patients and the controls for any of the five cytokines studied. Our study suggests that patch-stage mycosis fungoides is not determined by a specific genotype polymorphism. However, further studies on larger numbers of cases are needed before definite conclusions can be drawn.


Cochrane Database of Systematic Reviews | 2017

Interventions for the prevention of recurrent erysipelas and cellulitis.

Adam Dalal; Marina Eskin-Schwartz; Daniel Mimouni; Sujoy Ray; Walford Days; Emmilia Hodak; Leonard Leibovici; Mical Paul

BACKGROUNDnErysipelas and cellulitis (hereafter referred to as cellulitis) are common bacterial skin infections usually affecting the lower extremities. Despite their burden of morbidity, the evidence for different prevention strategies is unclear.nnnOBJECTIVESnTo assess the beneficial and adverse effects of antibiotic prophylaxis or other prophylactic interventions for the prevention of recurrent episodes of cellulitis in adults aged over 16.nnnSEARCH METHODSnWe searched the following databases up to June 2016: the Cochrane Skin Group Specialised Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, and LILACS. We also searched five trials registry databases, and checked reference lists of included studies and reviews for further references to relevant randomised controlled trials (RCTs). We searched two sets of dermatology conference proceedings, and BIOSIS Previews.nnnSELECTION CRITERIAnRandomised controlled trials evaluating any therapy for the prevention of recurrent cellulitis.nnnDATA COLLECTION AND ANALYSISnTwo authors independently carried out study selection, data extraction, assessment of risks of bias, and analyses. Our primary prespecified outcome was recurrence of cellulitis when on treatment and after treatment. Our secondary outcomes included incidence rate, time to next episode, hospitalisation, quality of life, development of resistance to antibiotics, adverse reactions and mortality.nnnMAIN RESULTSnWe included six trials, with a total of 573 evaluable participants, who were aged on average between 50 and 70. There were few previous episodes of cellulitis in those recruited to the trials, ranging between one and four episodes per study.Five of the six included trials assessed prevention with antibiotics in participants with cellulitis of the legs, and one assessed selenium in participants with cellulitis of the arms. Among the studies assessing antibiotics, one study evaluated oral erythromycin (n = 32) and four studies assessed penicillin (n = 481). Treatment duration varied from six to 18 months, and two studies continued to follow up participants after discontinuation of prophylaxis, with a follow-up period of up to one and a half to two years. Four studies were single-centre, and two were multicentre; they were conducted in five countries: the UK, Sweden, Tunisia, Israel, and Austria.Based on five trials, antibiotic prophylaxis (at the end of the treatment phase (on prophylaxis)) decreased the risk of cellulitis recurrence by 69%, compared to no treatment or placebo (risk ratio (RR) 0.31, 95% confidence interval (CI) 0.13 to 0.72; n = 513; P = 0.007), number needed to treat for an additional beneficial outcome (NNTB) six, (95% CI 5 to 15), and we rated the certainty of evidence for this outcome as moderate.Under prophylactic treatment and compared to no treatment or placebo, antibiotic prophylaxis reduced the incidence rate of cellulitis by 56% (RR 0.44, 95% CI 0.22 to 0.89; four studies; n = 473; P value = 0.02; moderate-certainty evidence) and significantly decreased the rate until the next episode of cellulitis (hazard ratio (HR) 0.51, 95% CI 0.34 to 0.78; three studies; n = 437; P = 0.002; moderate-certainty evidence).The protective effects of antibiotic did not last after prophylaxis had been stopped (post-prophylaxis) for risk of cellulitis recurrence (RR 0.88, 95% CI 0.59 to 1.31; two studies; n = 287; P = 0.52), incidence rate of cellulitis (RR 0.94, 95% CI 0.65 to 1.36; two studies; n = 287; P = 0.74), and rate until next episode of cellulitis (HR 0.78, 95% CI 0.39 to 1.56; two studies; n = 287). Evidence was of low certainty.Effects are relevant mainly for people after at least two episodes of leg cellulitis occurring within a period up to three years.We found no significant differences in adverse effects or hospitalisation between antibiotic and no treatment or placebo; for adverse effects: RR 0.87, 95% CI 0.58 to 1.30; four studies; n = 469; P = 0.48; for hospitalisation: RR 0.77, 95% CI 0.37 to 1.57; three studies; n = 429; P = 0.47, with certainty of evidence rated low for these outcomes. The existing data did not allow us to fully explore its impact on length of hospital stay.The common adverse reactions were gastrointestinal symptoms, mainly nausea and diarrhoea; rash (severe cutaneous adverse reactions were not reported); and thrush. Three studies reported adverse effects that led to discontinuation of the assigned therapy. In one study (erythromycin), three participants reported abdominal pain and nausea, so their treatment was changed to penicillin. In another study, two participants treated with penicillin withdrew from treatment due to diarrhoea or nausea. In one study, around 10% of participants stopped treatment due to pain at the injection site (the active treatment group was given intramuscular injections of benzathine penicillin).None of the included studies assessed the development of antimicrobial resistance or quality-of-life measures.With regard to the risks of bias, two included studies were at low risk of bias and we judged three others as being at high risk of bias, mainly due to lack of blinding.nnnAUTHORS CONCLUSIONSnIn terms of recurrence, incidence, and time to next episode, antibiotic is probably an effective preventive treatment for recurrent cellulitis of the lower limbs in those under prophylactic treatment, compared with placebo or no treatment (moderate-certainty evidence). However, these preventive effects of antibiotics appear to diminish after they are discontinued (low-certainty evidence). Treatment with antibiotic does not trigger any serious adverse events, and those associated are minor, such as nausea and rash (low-certainty evidence). The evidence is limited to people with at least two past episodes of leg cellulitis within a time frame of up to three years, and none of the studies investigated other common interventions such as lymphoedema reduction methods or proper skin care. Larger, high-quality studies are warranted, including long-term follow-up and other prophylactic measures.

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