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    236 results match your criteria Granuloma Faciale

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    Granuloma faciale: clinical, morphological and immunohistochemical aspects in a series of 10 patients.
    An Bras Dermatol 2016 Nov-Dec;91(6):803-807
    Universidade Estadual Paulista "Júlio de Mesquita Filho" (Unesp) - Botucatu (SP), Brazil.
    Granuloma faciale is a chronic, benign, cutaneous vasculitis with well-established clinical and morphological patterns, but with an unknown etiology. This study describes clinical and pathologic aspects of patients diagnosed with granuloma faciale. The authors analyzed demographic, clinical, morphological and immunohistochemical data from patients with a final diagnosis of granuloma faciale, confirmed between 1998 and 2012. Read More

    Disorders characterized by predominant or exclusive dermal inflammation.
    Semin Diagn Pathol 2016 Dec 14. Epub 2016 Dec 14.
    Section of Dermatopathology, Division of Surgical Pathology & Cytopathology, University of Virginia Medical Center, Room 3020 University of Virginia Hospital, 1215 Lee Street, Charlottesville, VA 22908-0214, USA. Electronic address:
    Some cutaneous inflammatory disorders are typified by a predominant or exclusive localization in the dermis. They can be further subdivided by the principal cell types into lymphocytic, neutrophilic, and eosinophilic infiltrates, and mixtures of them are also seen in a proportion of cases. This review considers such conditions. Read More

    Chronic Localized Fibrosing Leukocytoclastic Vasculitis Associated With Lymphedema, Intralymphatic and Intravascular Lymphocytosis, and Chronic Myelogenous Leukemia: A Case Report of Unilateral Erythema Elevatum Diutinum.
    Am J Dermatopathol 2016 Dec 7. Epub 2016 Dec 7.
    *Department of Pathology, Albany Medical College, Albany, NY; and †Departamento de Dermatología, Area de Dermatopatología, Hospital Luis Vernaza, Guayaquil, Ecuador.
    One of the pathogenic causes of cutaneous inflammatory pseudotumors is chronic localized fibrosing leukocytoclastic vasculitis (CLFLCV), a vasculitic reaction pattern seen in granuloma faciale (GF), a localized vasculitis, and erythema elevatum diutinum (EED), a generalized vasculitis. Patients with myelodysplastic syndromes (MDSs) are at risk for a diverse spectrum of cutaneous neutrophilic dermatoses such as EED. Herein, we report a 74-year-old man who presented with a large ulcerative, fungating tumor affecting the right flexor ankle caused by CLFLCV. Read More

    Nasal NK/T-cell lymphoma: A tragic case.
    Eur Ann Otorhinolaryngol Head Neck Dis 2017 Apr 24;134(2):121-122. Epub 2016 Oct 24.
    Service d'ORL et de Chirurgie Cervico-faciale, Hôpital 20-Août-1953, Casablanca, Morocco.
    Introduction: Nasal NK/T-cell lymphoma is a rare clinicopathological entity, formerly called midline lethal granuloma. Following progress in histology and the routine use of immunohistochemistry, nasal NK/T-cell lymphoma was recognized as a distinct entity by WHO in 2001.

    Case Report: The authors report the case of a 22-year-old, insulin-dependent diabetic woman, who presented with mid-facial inflammatory swelling following facial trauma, initially diagnosed and treated as cellulitis of the face. Read More

    [Differential diagnosis of basal cell carcinoma of the face: Dermatologist advice may avoid surgery].
    Rev Stomatol Chir Maxillofac Chir Orale 2016 Nov 14;117(5):335-339. Epub 2016 Jul 14.
    Aix Marseille université, 13916 Marseille, France; Service de dermatologie, hôpital Nord, AP-HM, 13915 Marseille cedex 20, France.
    Introduction: Basal cell carcinoma (BCC) is the most common skin cancer in France. It is commonly diagnosed in front of a papule or nodule of the face. The surgeon should be able to question the diagnosis of BCC when nodular lesions are untypical, keeping in mind that some differential diagnoses require only medical treatment. Read More

    Approach to cutaneous vasculitides with special emphasis on small vessel vasculitis: histopathology and direct immunofluorescence.
    Curr Opin Rheumatol 2017 Jan;29(1):39-44
    Department of Pathology, Acıbadem University, Istanbul, Turkey.
    Purpose Of Review: The present review will focus on recent publications in cutaneous vasculitides.

    Recent Findings: Some histopathological and clinical features, such as papillary dermal edema, perivascular C3 deposition, clinically evident edema, and lesions above the waist, may point out renal or gastrointestinal involvement in Henoch-Schönlein purpura (HSP). HSP associated with familial Mediterranean fever differs from typical isolated HSP by showing no deposits of IgA, much younger age, and location of the lesions on the face or the trunk. Read More

    Granuloma faciale treatment with tacrolimus.
    Dermatol Online J 2016 Jul 15;22(7). Epub 2016 Jul 15.
    Hospital Universitario Doctor Peset, Spain.
    We present a 40-year-old woman with a one-year history of a solitary and asymptomatic facial lesion. On physical examination a slightly infiltrated, smooth red to brown nodule was seen at the left malar region. A biopsy established the diagnosis of granuloma faciale. Read More

    Dermoscopy in General Dermatology: A Practical Overview.
    Dermatol Ther (Heidelb) 2016 Dec 9;6(4):471-507. Epub 2016 Sep 9.
    Department of Experimental and Clinical Medicine, Institute of Dermatology, University of Udine, Udine, Italy.
    Over the last few years, dermoscopy has been shown to be a useful tool in assisting the noninvasive diagnosis of various general dermatological disorders. In this article, we sought to provide an up-to-date practical overview on the use of dermoscopy in general dermatology by analysing the dermoscopic differential diagnosis of relatively common dermatological disorders grouped according to their clinical presentation, i.e. Read More

    Defining a new aggressiveness classification and using NFATc1 localization as a prognostic factor in cherubism.
    Hum Pathol 2016 Dec 3;58:62-71. Epub 2016 Aug 3.
    INSERM, UMRS 1138, Centre de Recherche de Cordeliers, Molecular Oral Pathology, 75006 Paris, France; Université Paris Descartes, 75006 Paris, France; APHP, Necker Enfants Malades, Service de Chirurgie Maxillo-Faciale et Plastique, 75015 Paris, France; APHP, CRMR des Malformations Rares de la Face et de la Cavité Buccale, 75015 Paris, France.
    Cherubism is a rare genetic disease characterized by bilateral giant cell reparative granuloma of the jaws consisting of a fibrotic stroma with giant multinucleated cells (GMCs) and osteoclastic features. Cherubism severity is highly variable, and recurrence after surgery is the most important risk. Currently, there are no prognostic indicators. Read More

    Granuloma faciale successfully treated with ingenol mebutate.
    Dermatol Ther 2016 Sep 30;29(5):325-329. Epub 2016 Jun 30.
    Department of Clinical and Molecular Sciences, Dermatological Unit and.
    Granuloma faciale (GF) is a rare chronic inflammatory dermatosis of unknown etiology, characterized by leukocitoclastic vasculitis usually occurring on the face. We report a case of 60-years-old man with 3 year history of multiple actinic keratoses (AK) and persistent asymptomatic erythematous papules and plaques located over his left temporal region and the cheek: histopathology was consistent with GF. Herein we describe the successful treatment of the lesion with ingenol mebutate 0. Read More

    Granuloma faciale: An unusual diascopic finding.
    Indian Dermatol Online J 2016 May-Jun;7(3):174-6
    Department of Skin and STD, Dr. BR Ambedkar Medical College, Bangalore, Karnataka, India.
    Granuloma faciale (GF) is a benign, chronic inflammatory disorder, characterized by reddish brown plaques with prominent follicular orificesand telangeictasia, usually occurring over the face. The condition often presents a problem in differential diagnosis. Herein we describe a case of GF with an unusual diascopic finding of an apple jelly appearance on diascopy. Read More

    A Concomitant Case of Orbital Granuloma Faciale and Eosinophilic Angiocentric Fibrosis.
    Ophthal Plast Reconstr Surg 2017 Mar/Apr;33(2):e47-e49
    Emory University School of Medicine, Atlanta, Georgia, U.S.A.
    Granuloma faciale is an eosinophilic dermatosis that typically presents as red-brown facial plaques of middle-aged white men, while eosinophilic angiocentric fibrosis is a histologically similar fibrotic condition affecting the respiratory mucosa. Both are very uncommon conditions and pose a therapeutic challenge. While a handful of reports have reported concurrent presentation, the authors present the first case of eyelid granuloma faciale with eosinophlilic angiocentric fibrosis. Read More

    "Drug-resistant granuloma faciale": treatment with carbon dioxide-GaAs laser.
    Dermatol Ther 2016 Sep 6;29(5):317-319. Epub 2016 Jun 6.
    ASL Viterbo, UOSD Dermatology, C.O.B. Belcolle, Italy.
    Granuloma faciale (GF), also known as "eosinophilic granuloma," is a rare benign leukocytoclastic vasculitis which most commonly occurs on the face of middle-aged Caucasian males. Clinically, GF appears as single or multiple, slowly growing, reddish-brown papules, nodules or plaques which may be cosmetically unpleasant. Its pathogenesis is unknown and GF is notoriously resistant to treatments. Read More

    Granuloma Faciale and Erythema Elevatum Diutinum in Relation to Immunoglobulin G4-Related Disease: An Appraisal of 32 Cases.
    Am J Clin Pathol 2016 Mar 2;145(3):401-6. Epub 2016 Mar 2.
    Departments of Dermatology, Pathology and Laboratory Medicine, Mayo Clinic College of Medicine, Rochester, MN.
    Objectives: To elucidate whether granuloma faciale (GF) and erythema elevatum diutinum (EED), two inflammatory skin dermatoses, meet the consensus histopathologic diagnostic criteria for immunoglobulin G4-related disease (IgG4-RD).

    Methods: With institutional review board approval, we assessed the clinical, microscopic, and immunophenotypic features of skin specimens of patients with GF and EED. We compared these findings with previously published consensus diagnostic criteria for IgG4-RD. Read More

    [NK/T-cell Lymphoma of nasal-type: A rare affection with a poor prognosis].
    Rev Stomatol Chir Maxillofac Chir Orale 2016 Jun 10;117(3):167-9. Epub 2016 Mar 10.
    Laboratoire d'anatomie et de cytologie pathologiques, hôpital Aristide le Dantec, Dakar, Sénégal.
    Introduction: NK/T cell lymphoma of nasal-type was described in 1933 as a malignant midfacial granuloma. The diagnosis of this rare affection is clinical and immunohistopathological. We report a case of NK/T cell lymphoma diagnosed at an advanced stage. Read More

    Cervicofacial non-tuberculous mycobacteria: A report of 30 cases.
    Eur Ann Otorhinolaryngol Head Neck Dis 2016 Apr 4;133(2):107-11. Epub 2016 Mar 4.
    Service d'ORL et chirurgie cervico-faciale, CHU de Nantes, 1, place Alexis-Ricordeau, 44000 Nantes, France. Electronic address:
    Background: Mycobacterial infection is the most common cause of cervical granuloma, implicating either a tuberculous or a non-tuberculous mycobacterium (NTM). NTM is a ubiquitous organism, found in soil, water, food, etc. The most frequently implicated is Mycobacterium avium-intracellular. Read More

    [Central giant cell granuloma in children: Presentation of different therapeutic options].
    Rev Stomatol Chir Maxillofac Chir Orale 2016 Jun 19;117(3):142-6. Epub 2016 Feb 19.
    Service de chirurgie maxillo-faciale, stomatologie et chirurgie plastique de la face, université d'Auvergne, NHE, CHU de Clermont-Ferrand, 1, place Lucie-Aubrac, 63003 Clermont-Ferrand, France; UMR Inserm/UdA, U1107, neuro-dol, trigeminal pain and migraine, faculté de chirurgie dentaire, BP 10448, 63000 Clermont-Ferrand, France; Faculté de médecine, université d'Auvergne, Clermont université, BP 10448, 63000 Clermont-Ferrand, France.
    Central giant cell granuloma (CGCG) is a benign tumor that may be subdivided in a non-aggressive form and an aggressive form. In aggressive forms, tumor size and high recurrence risk need large surgical resections. In order to minimize surgical morbidity, especially in children, medical treatments acting on the tumor proliferation are currently being assessed: steroids (triamcinolone), anti-osteoclastic drugs (calcitonine, alendronate, denosumab), anti-angiogenic drugs (interferon α). Read More

    Granuloma Faciale and Eosinophilic Angiocentric Fibrosis: Similar Entities in Different Anatomic Sites.
    Appl Immunohistochem Mol Morphol 2017 Mar;25(3):213-220
    Departments of *Pathology †Dermatology, Medical Sciences School, State University of Campinas (UNICAMP), Campinas, São Paulo, Brazil ‡Department of Dermatology, Ealing Hospital, London, UK.
    Background: Eosinophilic angiocentric fibrosis (EAF) and granuloma faciale (GF) share several histopathologic features, including eosinophil-rich inflammation, microangiitis, and progressive fibrosis. Concurrent presentation of EAF and GF suggests a pathogenetic link between them.

    Objectives: To identify histologic findings that tell them apart and construe the pathogenetic mechanisms behind each morphologic variable, 14 immunohistochemical markers were used to study the cells subpopulations in 14 cases of GF and 3 cases of EAF. Read More

    Eosinophilic Angiocentric Fibrosis of Sinonasal Region: A Rare & Under Reported Entity.
    J Clin Diagn Res 2015 Nov 1;9(11):ED05-6. Epub 2015 Nov 1.
    Professor and Head, Department of Pathology, Dayanand Medical College and Hospital , Ludhiana, Punjab, India .
    Eosinophilic angiocentric fibrosis is a rare pathology of the sinonasal tract and the upper respiratory system characterised by fibrosis with poorly understood pathogenesis. A 47-year-old male presented with a swelling over the dorsum of the nose. The possibility of fungal granuloma was being suggested on Magnetic Resonance Imaging (MRI). Read More

    Granuloma faciale: a good therapeutic response with the use of topical tacrolimus.
    An Bras Dermatol 2015 Sep-Oct;90(5):735-7
    Fundação Alfredo da Matta, Manaus, AM, Brasil.
    Granuloma faciale is a rare dermatosis of chronic course, benign, usually asymptomatic, first described in 1945 by Wingley. It is characterized by the appearance of well-defined, single or multiple papules, plaques and nodules, predominantly located in sun-exposed areas, especially the face. In this work we report the case of a female patient, 58 years old, evolving for ten years with multiple erythematous-brownish and asymptomatic papules on the face, whose histological examination confirmed the diagnosis of granuloma faciale. Read More

    [Our experience about the use of resorbable plates in the treatment of craniostenosis].
    Rev Stomatol Chir Maxillofac Chir Orale 2015 Sep 17;116(4):245-9. Epub 2015 Jul 17.
    Service de neurochirurgie pédiatrique, hôpital neurologique et neurochirurgical Pierre-Wertheimer, 69500 Lyon, France.
    Introduction: The use of resorbable plates increases for craniosynostosis surgery. This material, based on polymere (PLA, PGA) can replace steel wire and non resorbable plates. A few studies present surgical results about the use of this material with a long follow-up. Read More

    Treatment of Laser Resistant Granuloma Faciale with Intralesional Triamcinolone acetonide and 5-Fluorouracil Combination Therapy.
    J Cutan Aesthet Surg 2015 Apr-Jun;8(2):111-3
    Dermatology Institute of Victoria, Melbourne, Australia.
    This report describes a sixty year old male with biopsy proven Granuloma Faciale (GF). The patient had been unsuccessfully treated with multiple therapies. A mixture 0. Read More

    Laryngeal tuberculosis diagnosed by stool sample cultures: a case report.
    J Med Case Rep 2015 Mar 31;9:74. Epub 2015 Mar 31.
    Assistance Publique-Hôpitaux de Marseille, CHU Nord, Pôle Infectieux, Institut Hospitalo-Universitaire Méditerranée Infection, 13015, Marseille, France.
    Introduction: Laryngeal tuberculosis is a rare and often misdiagnosed disease. Its diagnosis is based on the association of a laryngeal lesion and the microbiological detection of Mycobacterium tuberculosis. Stool cultures have recently been described as a useful tool in the diagnosis of atypical forms of tuberculosis. Read More

    Eosinophilic Skin Diseases: A Comprehensive Review.
    Clin Rev Allergy Immunol 2016 Apr;50(2):189-213
    Department of Dermatology, The Second Xiangya Hospital, Central South University, 139 Middle Renmin Road, Changsha, Hunan, 410011, China.
    Eosinophilic skin diseases, commonly termed as eosinophilic dermatoses, refer to a broad spectrum of skin diseases characterized by eosinophil infiltration and/or degranulation in skin lesions, with or without blood eosinophilia. The majority of eosinophilic dermatoses lie in the allergy-related group, including allergic drug eruption, urticaria, allergic contact dermatitis, atopic dermatitis, and eczema. Parasitic infestations, arthropod bites, and autoimmune blistering skin diseases such as bullous pemphigoid, are also common. Read More

    Off-label use of TNF-alpha inhibitors in a dermatological university department: retrospective evaluation of 118 patients.
    Dermatol Ther 2015 May-Jun;28(3):158-65. Epub 2015 Mar 3.
    Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.
    Tumor necrosis factor-alpha (TNF)-alpha inhibitors are licensed for patients with severe refractory psoriasis and psoriatic arthritis. However, TNF-alpha inhibitors have also been used off-label for various recalcitrant mucocutaneous diseases. This study aimed to evaluate the efficacy and safety of TNF-alpha inhibitors used for off-label dermatological indications. Read More

    Chronic localized leukocytoclastic vasculitis: clinicopathological spectrum of granuloma faciale with and without extrafacial and mucosal involvement.
    G Ital Dermatol Venereol 2015 Feb 16;150(1):87-94. Epub 2015 Jan 16.
    Dermatology Unit, Department of Medical, Surgical Diagnostic and Pediatric Science, University of Pavia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy -
    Granuloma faciale (GF) is a rare cutaneous condition of unknown origin, that usually presents as one or more brown-purple papules, plaques and/or nodules, localized mostly on the face, although extrafacial lesions can also occur. Eosinophilic angiocentric fibrosis (EAF) is regarded as the mucosal counterpart of GF. Histologically, it has been described as a persistent leukocytoclastic vasculitis, with a dense polymorphous inflammatory infiltrate in the superficial and mid dermis, typically sparing the subpapillary dermis, the so called grenz zone. Read More

    The calcineurin inhibitor tacrolimus as a new therapy in severe cherubism.
    J Bone Miner Res 2015 May;30(5):878-85
    Institut National de la Santé et de la Recherche Médicale (INSERM) UMRS1138, Team Molecular Oral Pathophysiology, Cordeliers Research Center, University Paris-Diderot, University Paris-Descartes, and University Pierre and Marie Curie, Paris, France; Service de Chirurgie Maxillo-Faciale, Hôpital Necker Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; Unités de Formation et de Recherche (UFR) de Médecine Paris Descartes, Université Paris V, Paris, France; Centre de Références des Malformations de la Face et de la Cavité Buccale, Paris, France; Laboratoire de Physiopathologie Orale et Moléculaire, INSERM, UMRS 872, Equipe 5, Centre de Recherche des Cordeliers, Paris, France.
    Cherubism is a rare genetic disorder characterized by extensive growth of a bilateral granuloma of the jaws, resulting in facial disfigurement. Cherubism is caused by gain-of-function mutations in the SH3BP2 gene, leading to overactivation of nuclear factor of activated T cells, cytoplasmic 1 (NFATc1)-dependent osteoclastogenesis. Recent findings in human and mouse cherubism have suggested that calcineurin inhibitors might be drug candidates in cherubism medical treatment. Read More

    [Cryptococcosis: a potential aetiology of facial ulceration].
    J Mycol Med 2014 Dec;24(4):e185-8
    Service de dermatologie et de vénérologie, CHU Yalgado, Ouédraogo, Burkina Faso.
    Unlabelled: Cutaneous cryptococcosis is an uncommon aetiology of chronic facial ulceration but which may be associated to a potentially lethal focus of cryptococcosis.

    Observation: A 35-year-old AIDS patient under antiretroviral therapy, presented with a chronic facial ulceration. Histopathological examination of a biopsy of the facial ulceration showed an inflammatory granuloma and masses of yeasts. Read More

    Granuloma faciale treated with topical dapsone: a case report.
    Dermatol Online J 2014 Aug 17;20(8). Epub 2014 Aug 17.
    University of Connecticut School of Medicine.
    Granuloma faciale (GF) is an unusual, treatment-resistant skin disorder that commonly affects the face. Several medical and surgical interventions are available that offer varying degrees of benefit. Both the condition and the treatment modalities can lead to significant disfigurement. Read More

    [Parotid involvement in Churg-Strauss syndrome].
    Rev Stomatol Chir Maxillofac Chir Orale 2014 Jun 3;115(3):188-91. Epub 2014 May 3.
    Clinique de chirurgie maxillo-faciale et de stomatologie, centre hospitalier universitaire de Nantes, 1, place Alexis-Ricordeau, 44093 Nantes, France. Electronic address:
    Introduction: Churg-Strauss syndrome is a rare systemic vascularitis. This disease causes eosinophilic tissue infiltration. The most frequent manifestations are cortico-dependent asthma, mono- or polyneuropathy, paranasal sinus polyposis, and digestive and renal dysfunction. Read More

    Localized chronic fibrosing vasculitis in a tattoo: a unique adverse tattoo reaction.
    Am J Dermatopathol 2014 Apr;36(4):e81-3
    *University of Kansas School of Medicine, Kansas City, KS; †Division of Dermatology, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS; ‡Division of Infectious Diseases, Department of Internal Medicine, University of Kansas Medical Center, Kansas City, KS; and §Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS.
    Decorative tattoos are associated with a variety of adverse cutaneous reactions. We describe a unique fibrosing vasculitic reaction to red tattoo ink. The histopathology was similar to that in localized chronic fibrosing vasculitis (LCFV), but sharply limited to sites of red tattoo ink injection and associated with florid verrucoid epidermal hyperplasia. Read More

    Granuloma faciale: a rare disease from a dermoscopy perspective.
    An Bras Dermatol 2013 Nov-Dec;88(6 Suppl 1):97-100
    Federal University of São Paulo.
    The granuloma faciale is a rare and benign skin disease of unknown etiology, characterized by chronic leukocitoclastic vasculitis. It is characterized by skin lesions predominantly facial whose course is chronic and slowly progressive. The diagnosis is based on clinical features, histopathology and, more recently, in dermoscopy. Read More

    Postirradiation periocular granuloma faciale associated with uveitis.
    Ophthal Plast Reconstr Surg 2014 Jul-Aug;30(4):e92-5
    *Institute of Ophthalmology and Visual Science, †Department of Neurology and Neurosciences, and ‡Department of Pathology and Laboratory Medicine, Rutgers New Jersey Medical School, Newark, New Jersey, U.S.A.
    Granuloma faciale is a rare dermatopathologic condition that presents as brown-red plaques, nodules, or papules primarily on the face, with the potential for extrafacial and mucous membrane involvement. A case of an 83-year-old woman with periocular granuloma faciale accompanied by a marked anterior uveitis is presented; an association of periocular granuloma faciale with anterior uveitis has not been previously reported. Read More

    [Angiolymphoid hyperplasia with eosinophilia].
    Rev Stomatol Chir Maxillofac Chir Orale 2013 Nov 2;114(5):331-3. Epub 2013 May 2.
    Service d'ORL et de chirurgie maxillo-faciale, hôpital régional Mohamed Taher Maâmouri, Nabeul, Tunisie. Electronic address:
    Introduction: Angiolymphoid hyperplasia with eosinophilia (HALE) is a rare, benign proliferative vascular disorder of unknown etiology which typically presents as tumor-like nodules of the skin or subcutaneous tissue. It concerns mostly young female adults. We report a case of HALE located on the ear auricle diagnosed by biopsy. Read More

    [Medical indications for laser therapy in dermatology].
    Ned Tijdschr Geneeskd 2013 ;157(44):A6662
    Sint Franciscus Gasthuis, afd. Dermatologie, Rotterdam.
    Laser therapy in dermatology is often associated with cosmetic procedures. However, nowadays laser therapy has become a treatment modality for many dermatological diseases. We present three cases of patients with different dermatological diseases that are highly therapy-resistant. Read More

    Specificity of paediatric jawbone lesions: tumours and pseudotumours.
    J Craniomaxillofac Surg 2014 Mar 27;42(2):125-31. Epub 2013 May 27.
    APHP, Hôpital Necker Enfant Malades (Head of the Department: Vazquez), Service de chirurgie maxillo-faciale, Paris F75015, France; Université Paris 5, UFR médecine Paris Descartes, Paris F75006, France; Centre de références des malformations de la face et de la cavité buccale (Head of the Department: Vazquez), France; Laboratoire de Physiopathologie orale et Moléculaire (Head of the Department: Berdal), INSERM, UMRS 872, Equipe 5, Centre de recherche des Cordeliers, Paris 75006, France.
    Introduction: Characteristics and epidemiology of jaw tumours have been described mostly in adults. Compared with their adult counterparts, childhood jaw tumours show considerable differences. The aim of this study was to describe the different jaw tumours in children, define diagnostic tools to determine their specificity and describe optimal treatment. Read More

    The efficacy of pulsed dye laser treatment for inflammatory skin diseases: a systematic review.
    J Am Acad Dermatol 2013 Oct 24;69(4):609-615.e8. Epub 2013 May 24.
    Department of Dermatology, Amphia Hospital Breda, Breda, The Netherlands. Electronic address:
    Background: The position of the pulsed dye laser (PDL) in the treatment of inflammatory skin diseases is still unclear. Evidence-based recommendations are lacking.

    Objectives: We sought to systematically review all available literature concerning PDL treatment for inflammatory skin diseases and to propose a recommendation. Read More

    [Two cases of lymphoma in an implant capsule: A difficult diagnosis, an unknown pathology].
    Ann Chir Plast Esthet 2013 Dec 24;58(6):688-93. Epub 2013 May 24.
    Service de chirurgie plastique et maxillo-faciale, centre hospitalier Henri-Duffaut, 305, rue Raoul-Follereau, 84902 Avignon cedex 9, France. Electronic address:
    The anaplastic large cell lymphoma (ALCL) is a rare disease, its incidence in the United States is one case per 500,000 women and three for 100 million patients for breast single location. Forty-six cases have been reported in the literature. They can grow on any type of implant: expander prosthesis silicone and saline, smooth or textured envelope. Read More

    [Granulomatous invasive aspergillosis rhinosinusitis].
    J Mycol Med 2012 Dec 1;22(4):316-21. Epub 2012 Nov 1.
    Service ORL et chirurgie maxillo-faciale, hôpital La Rabta, Jabbari, 1007 Tunis, Tunisie.
    Introduction: Granulomatous invasive aspergillosis rhinosinusitis is a rare disease. Anatomopathologic and mycological examination allows the diagnosis. Treatment must be rapidly started in order to avoid orbital and intracranial complications. Read More

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