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2.
Colorectal Dis ; 14(11): 1418-23, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22390258

ABSTRACT

AIM: Retrorectal tumours are a rare and complex entity in adults and children. They present a varied symptomatology and their treatment is very different according to their histology. We aimed to evaluate our experience of tumours of the retrorectal space. METHOD: Forty patients with retrorectal tumours were divided into two groups according to age. The variables analysed were sex, signs and symptoms, complementary examinations, surgical approaches, adjuvant therapies, pathological analyses, recurrence and survival. RESULTS: Symptoms across the 30 adults varied--back pain (18) was the most common. Surgical intervention was performed on 20 patients; the rest were candidates for other treatments: five metastatic disease, two lymphomas and two Ewing tumour. The most common surgical approach was posterior, with 10 cases (50%). In all, 70% of adult tumours were malignant, with chordoma (30%) and metastases (20%) being the most common lesions. The most frequent benign lesion was hamartoma (10%). The 1- and 5-year mortality rates were 23.8% and 38.1%, respectively. In the paediatric group, three patients were diagnosed in utero. The symptoms among children varied and all were operated upon. The most frequent tumour was teratoma. Overall mortality was 20%. CONCLUSIONS: Given their complexity, these tumours should be addressed by experts and all treatment options must be contemplated. They continue to present a challenge, above all in malignant tumours where the tumour cannot be controlled at a locoregional level.


Subject(s)
Digestive System Surgical Procedures/methods , Rectal Neoplasms , Academic Medical Centers , Adolescent , Adult , Child , Female , Humans , Male , Middle Aged , Pregnancy , Prenatal Diagnosis , Rectal Neoplasms/classification , Rectal Neoplasms/diagnosis , Rectal Neoplasms/surgery , Spain
3.
Thorax ; 54(6): 558-60, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10335014

ABSTRACT

Antileukotriene drugs are new therapeutic agents that have recently been approved for the treatment of asthma. Several cases of eosinophilic conditions including Churg-Strauss syndrome have been reported to be associated with zafirlukast, a cysteinyl leukotriene type 1 receptor antagonist. So far no other leukotriene modifier has been associated with the syndrome. The case history is presented of a man with allergic rhinitis and asthma who had received intermittent pulse therapy with oral corticosteroids. Pulmonary eosinophilia developed while he was receiving treatment with montelukast, a chemically distinct cysteinyl leukotriene type 1 receptor antagonist. After discontinuation of montelukast therapy and administration of systemic corticosteroids the patient's symptoms reversed rapidly and there was prompt resolution of the pulmonary infiltrates. We believe that cysteinyl leukotriene type 1 receptor antagonists are safe and effective drugs for most patients with asthma but caution is needed for those with more severe disease who require systemic corticosteroids, especially if they show characteristics of the atypical allergic diathesis seen in the prodromal phase of Churg-Strauss syndrome.


Subject(s)
Acetates/adverse effects , Anti-Asthmatic Agents/adverse effects , Asthma/drug therapy , Leukotriene Antagonists/adverse effects , Pulmonary Eosinophilia/chemically induced , Quinolines/adverse effects , Adult , Churg-Strauss Syndrome/diagnosis , Cyclopropanes , Fever/chemically induced , Humans , Male , Pulmonary Eosinophilia/diagnosis , Respiratory Sounds/etiology , Sulfides
4.
Prenat Diagn ; 15(9): 859-63, 1995 Sep.
Article in English | MEDLINE | ID: mdl-8559758

ABSTRACT

A large intrapericardial teratoma was found at necropsy in a 38-week stillborn fetus, in which prenatal diagnosis of hydrops fetalis and an echogenic cardiac mass had been made. Clinical and pathological data are reported. In utero intrapericardial teratomata lead to different outcomes depending on whether fetal hydrops is associated. When generalized fetal hydrops is not present, the outcome is good, even in cases with large pericardial effusions. When generalized fetal hydrops occurs, it often results in a poor outcome. In our literature review, we have found eight perinatal deaths in nine similar cases reported.


Subject(s)
Fetal Diseases/diagnostic imaging , Heart Neoplasms/complications , Hydrops Fetalis/complications , Pericardium , Teratoma/complications , Adult , Cordocentesis , Female , Heart Neoplasms/diagnostic imaging , Humans , Hydrops Fetalis/diagnostic imaging , Male , Pericardium/diagnostic imaging , Pericardium/pathology , Pregnancy , Teratoma/diagnostic imaging , Ultrasonography, Prenatal
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