R. Caputo

Memorial Sloan Kettering Cancer Center

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Emilio Berti

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Angelo Valerio Marzano

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

S. Cavicchini

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Elvio Alessi

University of Milan

Stefano Veraldi

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Ramón Grimalt

Universitat Internacional de Catalunya

Stefano Cambiaghi

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Raffaele Gianotti

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Gianluca Tadini

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

M. Monti

University of Milan

Cooperative Institutions

University of Milan

206

Istituti di Ricovero e Cura a Carattere Scientifico

132

Ospedale Maggiore

119

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

105

Advanced Dermatology

Institute of Dermatology

Inserm

University Dermatology

Assistance Publique – Hôpitaux de Paris

Université Paris Cité

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Clinical efficacy and safety comparison of adapalene gel and tretinoin gel in the treatment of acne vulgaris: Europe and U.S. multicenter trials

Journal of the American Academy of Dermatology (1997)

W.J. Cunliffe R. Caputo Brigitte Dréno L Förström M. Heenen

Adapalene

Tretinoin

10.1016/s0190-9622(97)70056-2

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Citations (97)

La terapia dell'acne con una associazione norelgestromina-etinilestradiolo

R. Caputo Mattia Barbareschi

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Citations (0)

Reticular Erythematous Mucinosis Occurring in a Brother and Sister

Dermatology (2006)

R. Caputo Angelo Valerio Marzano Athanasia Tourlaki Maurizio Marchini

Reticular erythematous mucinosis (REM) is a rare, primary cutaneous mucinosis clinically characterized by a persistent reticular erythema on the mid chest and mid-upper back, and histologically by a mononuclear cell infiltrate and deposits of mucin in the dermis. To our knowledge, the present report of REM occurring in a Caucasian man and his sister is the first reported case of familial REM. Since a host-specific immune response to unknown antigens may be involved in the pathogenesis of this entity, human leukocyte antigen typing was determined and compared to those reported in autoimmune diseases.

Reticular connective tissue

Mucinosis

Reticular Dermis

Sister

Erythema

10.1159/000092293

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Citations (20)

[Skin manifestations of the Rosai-Dorfman syndrome].

PubMed (1984)

Avril Mf Amiel Jl C Théodore Georges Chahine Caillaud Jm

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Citations (7)

Internal Organization of Plasma Membranes during the Acantholytic Process. A Freeze‐Fracture Study

Journal of Cutaneous Pathology (1980)

R. Caputo Marco Innocenti Giulio Gasparini

The internal organization of plasma membranes was studied in seven subjects with pemphigus vulgaris and in one subject with familial pemphigus using the freeze‐fracture technique. The results obtained seem to suggest that the acantholytic process is produced in a similar fashion whatever the pathogenic agent and that desmosomes represent the “target” membrane specializations in the acantholytic phenomena. The reduction and eventual disappearance of desmosomal particle aggregations is seemingly accompanied by an increase in gap junctions.

10.1111/j.1600-0560.1980.tb01184.x

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Citations (7)

Ultrastructural changes in the epidermis of xeroderma pigmentosum lesions in various stages of development

Archives of Dermatological Research (1971)

R. Caputo Andrea Califano

Epidermis (zoology)

Basal (medicine)

10.1007/bf00595268

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Citations (7)

Subject Index Vol. 212, 2006

Dermatology (2006)

Zhi Yang Haijing Yu Baoweng Cheng Wenru Tang Yongli Dong

200 Chlamydia trachomatis 41 Chlorhexidine 21 (S), 91 (S), 109 (S) Chromosome aberration 94 (S) Chronic actinic dermatitis 377 -renal failure 89 Cicatricial alopecia 400 c-Kit mutation 70 Cleaning protocols 4 (S) Collagen, type VII 381 Colorectal surgery 53 (S) Compatibility with PVP-I disinfectants 58 (S) Complete remission 93 Computer, side-eff ect 392 Congenital melanocytic nevus, dermoscopic features 354 Congenital nevus 198 Conjunctival lymphoma 93 Consecutive complete lymph node dissection 47 Contact dermatitis, irritant 235 -therapy, short 235 Corneocyte 23 Coronavirus 119 (S) Cost of illness 137 Coverfl ex 66 Cutaneous drug reaction 59 -mucinosis 385 Cytotoxicity 91 (S)

10.1159/000093447

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Citations (0)

Olmsted Syndrome in Twins

Archives of Dermatology (1995)

Stefano Cambiaghi Gianluca Tadini Mauro Barbareschi R. Caputo

Olmsted syndrome is a rare disorder of keratinization appearing at birth or in early infancy that is characterized by the unusual association of palmoplantar keratoderma and periorificial hyperkeratosis, with possible involvement of other ectodermal derivatives.^1-6We report the second familial case, showing a progressive course unresponsive to conventional treatment.

Report of a Case.

The patients are monozygotic male twins, born at term to nonconsanguineous parents, aged 29 (father) and 25 (mother) years. At 4 months of age, both children developed bilateral palmoplantar keratoderma and keratotic lesions at the external acoustic meatus. Familial history was negative for any related skin disorders. Examination at age 15 months showed symmetrical, thick, sharply marginated, and yellowish areas of hyperkeratosis affecting the plantar surface of the forefeet and of the first and fifth toes. The lesions were surrounded by an erythematous border and extended onto the lateral aspects of the toes. A periodic complete

Keratoderma

Palmoplantar keratoderma

Dyskeratosis

10.1001/archderm.1995.01690180118028

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Citations (39)

Erratum

Dermatology (2005)

C.E.M. Griffiths M. Lebwohl G.G. Krueger Ichiro Katayama Kiyoshi Nishioka

10.1159/000088815

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Citations (0)

Amicrobial Pustular Dermatosis of Cutaneous Folds Associated with Autoimmune Disorders: A New Entity?

Dermatology (1996)

Angelo Valerio Marzano F. Capsoni Emilio Berti Giulio Gasparini S. Bottelli

Background: An unclassified amicrobial pustular dermatosis particularly affecting the main cutaneous folds, external auditory canals and scalp and coexisting with systemic lupus erythematosus has been recently described. Objective: We studied 3 young females bearing such cutaneous manifestations in association with subacute cutaneous lupus erythematosus, celiac disease and various serum autoantibodies, respectively, in order to further characterize this possibly new entity. Methods: Various routine and immunological laboratory tests, histopathologic and direct immunofluorescence examinations and in vitro studies of neutrophil function were performed in each patient. Results: We reported our findings and compared our cases with the few others appearing in the literature. We documented an impaired neutrophil chemotaxis in 2 subjects, but neutrophil dysfunction does not seem to be one of the verifying criteria. Conclusions: All of these cases may represent a distinctive form in the clinicopathological spectrum of neutrophilic dermatoses (ND) because of the typical distribution and the close link with different autoimmune disorders. Cimetidine in combination with ascorbic acid can be indicated as an effective and safe alternative to the classic medications of ND, although the action of both drugs remains unexplained.

10.1159/000246219

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Citations (45)