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Dive into the research topics where Paola Monari is active.

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Featured researches published by Paola Monari.


Dermatology | 2007

Borrelia burgdorferi-Associated Primary Cutaneous Marginal-Zone B-Cell Lymphoma: A Case Report

Paola Monari; Camillo Farisoglio; P Calzavara Pinton

An association between Borrelia burgdorferi with primary cutaneous B-cell lymphoma (PCBCL) has long been suspected but just recently, thanks to a polymerase chain reaction technique, it had been possible to demonstrate B. burgdorferi-specific DNA in skin lesions of patients with different PCBCL subtypes. Locating cases of PCBCL that are related to B. burgdorferi infection could be really important for therapeutic implications; in fact, there are several reports of PCBCL responding to antibiotic therapy against B. burgdorferi. We report a case of B. burgdorferi-associated primary cutaneous marginal-zone B-cell lymphoma that, after specific antimicrobial therapy, did not show any clinical regression. We can conclude that additional studies are necessary in order to establish the use of antimicrobial therapy in B. burgdorferi-associated PCBCL.


Dermatologic Therapy | 2009

Cutaneous lesions as initial signs of interferon α-induced sarcoidosis: report of three new cases and review of the literature

F. Fantini; Claudia Padalino; Giulio Gualdi; Paola Monari; Alberto Giannetti

Sarcoid reactions are well‐recognized adverse events during interferon (IFN) therapy. They are frequently underdiagnosed because misinterpreted as IFN‐induced side effects. Sarcoid cutaneous lesions may therefore represent useful hints to an early diagnosis, but their incidence is unknown. We report three new cases of mono‐localized, purely cutaneous IFNα‐induced sarcoidosis. In addition, an extensive review of the literature, with special attention to skin involvement, was performed through a PubMed search. The analysis of the retrieved articles showed that cutaneous lesions are frequent signs of IFN‐induced sarcoidosis. Skin involvement is documented in 56% of the reports and it appears among the presenting and diagnostic signs of a sarcoid reaction in 51%. Special attention to dermatologic signs is imperative in the course of IFN therapy because even minimal skin involvement may offer a clue to an early diagnosis of IFN‐induced sarcoidosis.


British Journal of Dermatology | 2012

Successful treatment of systemic cold contact urticaria with etanercept in a patient with psoriasis.

Giulio Gualdi; Paola Monari; M.T. Rossi; Silvia Crotti; Piergiacomo Calzavara-Pinton

mastocytoma: an uncommon variant mimicking juvenile xanthogranuloma and Langerhans cell histiocytosis. J Cutan Pathol 2009; 36:1215–20. 9 Sotlar K, Cerny-Reiterer S, Petat-Dutter K et al. Aberrant expression of CD30 in neoplastic mast cells in high-grade mastocytosis. Mod Pathol 2011; 24:585–95. 10 Valent P, Sotlar K, Horny HP. Aberrant expression of CD30 in aggressive systemic mastocytosis and mast cell leukemia: a differential diagnosis to consider in aggressive hematopoietic CD30positive neoplasms. Leuk Lymphoma 2011; 52:740–4.


Photodermatology, Photoimmunology and Photomedicine | 2010

Merkel cell carcinoma arising in immunosuppressed patients treated with high-dose ultraviolet A1 (320–400 nm) phototherapy: a report of two cases

Piergiacomo Calzavara-Pinton; Paola Monari; Ausilia Maria Manganoni; Marco Ungari; M.T. Rossi; Giulio Gualdi; Marina Venturini; Raffaella Sala

Merkel cell carcinoma (MCC) is an aggressive neuroendocrine tumour of the skin. Though immunodeficiency is the most relevant risk factor, ultraviolet (UV) radiation is also involved, but as of yet we do not know the action spectrum, pattern or dose which would produce a dangerous exposure. A retrospective study of two immunosuppressed patients who developed MCC during, or soon after a treatment cycle with high dose UVA1 exposures was conducted, in order to understand wether repeated exposures to suberythemogenic UVA1 radiation may have a cancerogenic activity provoking MCC in immunosuppressed patients.


Journal of The European Academy of Dermatology and Venereology | 2010

Electrochemotherapy-induced virus disappearance in HHV-8-positive skin nodules of Kaposi sarcoma: first histological and immunohistochemical demonstration of efficacy

Giulio Gualdi; Paola Monari; F. Fantini; A.M. Cesinaro; A Cimitan

and rapid resolution of GA following discontinuation of topiramate. Although the temporal relationship between drug discontinuation and skin resolution is evident, further studies and epidemiological data are necessary to support our clinical observation. Based on the T-cell subpopulations identified in GA lesions, we hypothesize that a delayed-type hypersensitivity reaction to topiramate was the involved pathogenetic factor.


Journal of The European Academy of Dermatology and Venereology | 2015

Matter of margins

Giulio Gualdi; Paola Monari; Silvia Crotti; G. Damiani; Fabio Facchetti; Piergiacomo Calzavara-Pinton; F. Fantini

Basal cell carcinoma (BCC) is the most common cancer, it represents a significant economic burden to health services because of a large volume of affected patients. Surgical excision with histological assessment of the surgical margins is widely considered as the mainstay of BCC treatment. Incomplete removal, in fact, should be considered a poor prognostic indicator, as incomplete removal of lesions is at risk of local recurrence. Actually, dermatological surgeries are carried out by a variety of different types of practitioners, such as plastic surgeons, maxillofacial surgeons, otorhinolaryngologists, ophthalmologists and finally dermatologists. Incomplete removal of the tumour ranges from 6.3% to 25%, depending on the improper intra‐operative evaluation of the extent of the tumour. It depends on the clinical knowledge derived from both training and daily experience. In this sense, the majority of the largest studies derive from plastic surgeons, while dermatologists have small case series, albeit with a higher therapeutic efficacy in terms of complete surgical excision.


Journal of The European Academy of Dermatology and Venereology | 2007

Sentinel lymph node biopsy in clear cell sarcoma.

F. Fantini; Paola Monari; S Bassissi; Antonio Maiorana; A.M. Cesinaro

© 2007 The Authors 1271 JEADV 2007, 21, 1253–1302 Journal compilation


British Journal of Dermatology | 2015

Eruptive squamous cell carcinomas with keratoacanthoma‐like features in a patient treated with ruxolitinib

A. Fabiano; Piergiacomo Calzavara-Pinton; Paola Monari; E. Moggio; Giovanni Pellacani; A.M. Manganoni; Giulio Gualdi

1 Asbrink E, Hovmark A. Serum IgE levels in patients with bullous pemphigoid and its correlation to the activity of the disease and anti-basement membrane zone antibodies. Acta Derm Venereol 1984; 64:243–6. 2 Rico MJ, Benning C, Weingart ES et al. Characterization of skin cytokines in bullous pemphigoid and pemphigus vulgaris. Br J Dermatol 1999; 140:1079–86. 3 Schroeder JT, MacGlashan DW, Lichtenstein LM. Human basophils: mediator release and cytokine production. Adv Immunol 2001; 77:93–122. 4 Sokol CL, Barton GM, Farr AG, Medzhitov R. A mechanism for the initiation of allergen-induced T helper type 2 responses. Nat Immunol 2008; 9:310–18. 5 Yoshimoto T, Yasuda K, Tanaka H et al. Basophils contribute to TH2-IgE responses in vivo via IL-4 production and presentation of peptide-MHC class II complexes to CD4 + T cells. Nat Immunol 2009; 10:706–12. 6 Motomura Y, Morita H, Moro K et al. Basophil-derived interleukin-4 controls the function of natural helper cells, a member of ILC2s, in lung inflammation. Immunity 2014; 40:758–71. 7 Charles N, Hardwick D, Daugas E et al. Basophils and the T helper 2 environment can promote the development of lupus nephritis. Nat Med 2010; 16:701–7. 8 Agis H, Krauth MT, B€ ohm A et al. Identification of basogranulin (BB1) as a novel immunohistochemical marker of basophils in normal bone marrow and patients with myeloproliferative disorders. Am J Clin Pathol 2006; 125:273–81. 9 Ito Y, Satoh T, Takayama K et al. Basophil recruitment and activation in inflammatory skin diseases. Allergy 2011; 66:1107–13. 10 Kasperkiewicz M, Zillikens D. The pathophysiology of bullous pemphigoid. Clin Rev Allergy Immunol 2007; 33:67–77.


Journal of Dermatological Case Reports | 2010

Multiple eruptive clear cell acanthoma.

Paola Monari; Camillo Farisoglio; Giulio Gualdi; Giorgio Botali; Marco Ungari; Piergiacomo Calzavara-Pinton

BACKGROUND Clear cell acanthoma is a rare solitary benign epidermal tumor of unknown etiology. The disease arises in the middle-age, with no sex predominance. It appears as a single reddish papule or papule-nodule and a peripheral scaling collarette is characteristic. Although solitary lesions are the rule, less than 30 cases of multiple Clear cell acanthoma have been described in the literature to date. MAIN OBSERVATIONS We report an unusual case of a healthy 74-year-old male with multiple clear cell acanthoma on the lower extremities treated successfully with cryotherapy. CONCLUSIONS Despite significant progress in treatment of clear cell acanthoma, cryotherapy, based on liquid nitrogen, remains an important alternative in treating multiple clear cell acanthomas.


International Wound Journal | 2011

Nested graft in chronic wounds: a new solution for an old problem.

Giulio Gualdi; Paola Monari; Camillo Farisoglio; Piergiacomo Calzavara-Pinton

It is well shown that chronic wounds are populated by cells unable to respond to re‐epithelising stimulus. Large ulcers that remain unhealed for several months are more difficult to treat probably because of the depletion of active factors. Yet in 1869 Reverdin realised that the partial coverage of an ulcer with small fragments of healthy skin was able to lead to wound healing; unfortunately, its employment was limited to granulating wounds. Recently, the importance of factors such as cytokines, chemokines and adhesion molecules in wound healing, and the involvement of all cellular types resident or transiting in the skin has been partially elucidated. In this study, we proposed to simultaneously provide a new cellular and molecular reservoir with the efficient stimulus to trigger it. We created receiving site inside the ulcer, able to contain a full‐thickness graft taken from a donor site. Our aim was not to cover the entire defect, but to use the minigraft as ‘fount’ of functional cells and to give an acute stress through the chambers created inside the ulcer. A complete wound healing was obtained in all patients treated in a short period of time. This technique does not require special equipment and assistance in maintaining costs at very low levels.

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F. Fantini

University of Modena and Reggio Emilia

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A. Lallas

Aristotle University of Thessaloniki

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A.M. Cesinaro

University of Modena and Reggio Emilia

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