B Cornia

University of Bologna

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Co-Authors

M Schiavina

Policlinico S.Orsola-Malpighi

Maurizio Zompatori

University of Bologna

Giampaolo Gavelli

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori

A Fabiani

Policlinico S.Orsola-Malpighi

C Sturani

Hesperia Hospital

Venerino Poletti

University of Bologna

S Pileri

European Institute of Oncology

Romeo Canini

Policlinico S.Orsola-Malpighi

Piloni

Istituti di Ricovero e Cura a Carattere Scientifico

M. Miglioli

Pontifícia Universidade Católica do Paraná

Cooperative Institutions

University of Bologna

Policlinico S.Orsola-Malpighi

Istituti di Ricovero e Cura a Carattere Scientifico

Medica (Italy)

Ospedale Bellaria

Istituto di Ematologia di Bologna

Azienda USL di Bologna

Université Paris Cité

Hôtel-Dieu de Paris

Research Institute of Radiology

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[Radiological diagnosis of pulmonary arterial hypertension in idiopathic pulmonary fibrosis].

PubMed (1984)

Giampaolo Gavelli Maurizio Zompatori C Sturani B Cornia S Pileri

Neuroradiology

Cardiac catheterization

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Citations (0)

Bronchopulmonary Involvement in Ulcerative Colitis

Journal of Clinical Gastroenterology (1990)

Paolo Gionchetti M Schiavina Massimo Campieri A Fabiani B Cornia

We report two cases of pulmonary involvement in ulcerative colitis. The first patient, a 37-year-old woman, had bilateral basal bronchiectasis full of mucopurulent secretion, with a marked improvement of pulmonary function and roentgenographic appearance after a conservative approach. The second patient had severe pulmonary fibrosis of autoimmune nature and died owing to a pulmonary infection. In the second patient, a sulfasalazine reaction as an etiologic factor was excluded, while in the first this possibility seemed unlikely. Therefore, we take these two cases as examples of the extraintestinal manifestations of ulcerative colitis.

Sulfasalazine

Mesalazine

10.1097/00004836-199012000-00010

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Citations (27)

[The correlation between radiological and haemodynamic pictures in the diagnosis of pulmonary hypertension in chronic obstructive diseases (author's transl)].

PubMed (1978)

Giampaolo Gavelli B Cornia Maurizio Zompatori Piloni M Schiavina

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Lymphangioleiomyomatosis: clinical course.

PubMed (1994)

M Schiavina A Fabiani B Cornia E DeBenedictis Venerino Poletti

Pulmonary lymphangioleiomyomatosis (LAM) is a rare disease of smooth muscle proliferation that generally leads to death, due to respiratory failure, within 10 yrs. The disease almost exclusively affects women of child-bearing age and rarely in postmenopausal years. High resolution computed tomographic (CT) patterns are characteristic and almost pathognomonic for LAM. Attempts to treat this disease with hormonal therapy have shown that a number of hormonal manipulations may not be helpful, but that surgical or radiant oophorectomy alone is the most effective treatment, even if the disease is so rare as to preclude randomized trials. Castration, as a means of early therapy, has been associated with a stable respiratory picture in our patients.

Pathognomonic

Lymphangioleiomyomatosis

Rare disease

Hormonal Therapy

Oophorectomy

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Citations (2)

Lymphangioleimyomatosis: Clinical course

Monaldi Archives for Chest Disease - Cardiac Series (1994)

M Schiavina A Fabiani B Cornia Erika A. DeBenedictis Venerino Poletti

Course (navigation)