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1.
Radiol Bras ; 55(2): 128-133, 2022.
Article in English | MEDLINE | ID: mdl-35414729

ABSTRACT

Cystic echinococcosis (hydatid disease) is a zoonotic parasitic disease, caused by ingestion of Echinococcus granulosus eggs, that can result in cyst formation anywhere on the body. Hydatid disease is frequently seen in regions where there is human-animal contact and poor socioeconomic development. The prevalence of the disease ranges from 0 to 79 cases/100,000 population. Hydatid cysts are typically found in the liver and lungs, being less common in other parts of the body. Computed tomography or magnetic resonance imaging is often used in order to clarify the sites affected by a hydatid cyst, such as the cranial and thoracic regions, which also facilitates the surgical evaluation and minimizes complications. Although rare, hydatid cysts in atypical locations can provoke unusual complications, with unpredictable findings and symptoms. This essay discusses the radiological aspects of rare thoracic hydatid cysts.


A equinococose cística (doença hidática) é uma doença parasitária zoonótica causada pela ingestão de ovos de Echinococcus granulosus, que pode resultar na formação de cistos em qualquer parte do corpo. A doença hidática é frequentemente vista em regiões onde há contato humano-animal e baixo desenvolvimento socioeconômico. A prevalência da doença varia de 0 a 79 casos/100.000 habitantes. Os cistos hidáticos são normalmente encontrados no fígado e nos pulmões, sendo menos comuns em outras partes do corpo. A tomografia computadorizada ou a ressonância magnética são frequentemente utilizadas para indicar os locais afetados por um cisto hidático, como as regiões craniana e torácica, o que também facilita a avaliação cirúrgica e minimiza complicações. Embora raros, os cistos hidáticos em locais atípicos podem provocar complicações incomuns, com achados e sintomas imprevisíveis. Este ensaio discute os aspectos radiológicos dos raros cistos hidáticos no tórax.

2.
Radiol. bras ; 55(2): 128-133, mar.-abr. 2022. graf
Article in English | LILACS-Express | LILACS | ID: biblio-1365295

ABSTRACT

Abstract Cystic echinococcosis (hydatid disease) is a zoonotic parasitic disease, caused by ingestion of Echinococcus granulosus eggs, that can result in cyst formation anywhere on the body. Hydatid disease is frequently seen in regions where there is human-animal contact and poor socioeconomic development. The prevalence of the disease ranges from 0 to 79 cases/100,000 population. Hydatid cysts are typically found in the liver and lungs, being less common in other parts of the body. Computed tomography or magnetic resonance imaging is often used in order to clarify the sites affected by a hydatid cyst, such as the cranial and thoracic regions, which also facilitates the surgical evaluation and minimizes complications. Although rare, hydatid cysts in atypical locations can provoke unusual complications, with unpredictable findings and symptoms. This essay discusses the radiological aspects of rare thoracic hydatid cysts.


Resumo A equinococose cística (doença hidática) é uma doença parasitária zoonótica causada pela ingestão de ovos de Echinococcus granulosus, que pode resultar na formação de cistos em qualquer parte do corpo. A doença hidática é frequentemente vista em regiões onde há contato humano-animal e baixo desenvolvimento socioeconômico. A prevalência da doença varia de 0 a 79 casos/100.000 habitantes. Os cistos hidáticos são normalmente encontrados no fígado e nos pulmões, sendo menos comuns em outras partes do corpo. A tomografia computadorizada ou a ressonância magnética são frequentemente utilizadas para indicar os locais afetados por um cisto hidático, como as regiões craniana e torácica, o que também facilita a avaliação cirúrgica e minimiza complicações. Embora raros, os cistos hidáticos em locais atípicos podem provocar complicações incomuns, com achados e sintomas imprevisíveis. Este ensaio discute os aspectos radiológicos dos raros cistos hidáticos no tórax.

3.
Ther Clin Risk Manag ; 13: 1085-1089, 2017.
Article in English | MEDLINE | ID: mdl-28894371

ABSTRACT

INTRODUCTION: Chest trauma may be blunt or penetrating and the chest is the third most common trauma region. It is a significant cause of mortality. Multidetector computed tomography (MDCT) has been an increasingly used method to evaluate chest trauma because of its high success in detecting tissue and organ injuries. Herein, we aimed to present MDCT findings in patients with blunt and penetrating chest trauma admitted to our department. METHODS: A total of 240 patients admitted to the emergency department of our hospital between April 2012 and July 2013 with a diagnosis of chest trauma who underwent MDCT evaluations were included. Most of the patients were male (83.3%) and victims of a blunt chest trauma. The images were analyzed with respect to the presence of fractures of bony structures, hemothorax, pneumothorax, mediastinal organ injury, and pulmonary and vascular injuries. RESULTS: MDCT images of the 240 patients yielded a prevalence of 41.7% rib fractures, 11.2% scapular fractures, and 7.5% clavicle fractures. The prevalence of thoracic vertebral fracture was 13.8% and that of sternal fracture was 3.8%. The prevalence of hemothorax, pneumothorax, pneumomediastinum, and subcutaneous emphysema was 34.6%, 62.1%, 9.6%, and 35.4%, respectively. The prevalence of rib, clavicle, and thoracic vertebral fractures and pulmonary contusion was higher in the blunt trauma group, whereas the prevalence of hemothorax, subcutaneous emphysema, diaphragmatic injury, and other vascular lacerations was significantly higher in the penetrating trauma group than in the blunt trauma group (p<0.05). CONCLUSION: MDCT images may yield a high prevalence of fracture of bony structures, soft tissue lacerations, and vascular lesions, which should be well understood by radiologists dealing with trauma.

4.
Ther Clin Risk Manag ; 13: 939-943, 2017.
Article in English | MEDLINE | ID: mdl-28794637

ABSTRACT

BACKGROUND: Mediastinoscopy is a good method to evaluate mediastinal lesions. We sought to determine the current role of mediastinoscopy in the investigation of non-lung cancer patients with mediastinal lymphadenopathy. MATERIALS AND METHODS: We retrospectively reviewed clinical parameters (age, gender, histological diagnosis, morbidity, mortality) of all patients without lung cancer who consecutively underwent mediastinoscopy in Hospital of Faculty of Medicine of Dicle University between June 2003 and December 2016. RESULTS: Two-hundred twenty nine patients without lung cancer who underwent mediastinoscopy for the pathological evaluation of mediastinum during the study period were included. There were 156 female (68%) and 73 male (32%) patients. Mean age was 52.6 years (range, 16 to 85 years). Mean operative time was 41 minutes (range, 25 to 90 minutes). Mean number of biopsies was 9.3 (range, 5 to 24). Totally, 45 patients (19.6%) had previously undergone a nondiagnostic bronchoscopic biopsy such as transbronchial needle aspiration or endobronchial ultrasound-guided transbronchial needle aspiration. Mediastinoscopy was diagnostic for all patients. Diagnosis included sarcoidosis (n=100), tuberculous lymphadenitis (n=66), anthracosis lymphadenitis (n=44), lymphoma (n=11) metastatic carcinoma (n=5), and Castleman's disease (n=1); there was a diagnosis of silicosis in one patient and tymoma in one patient. Neither operative mortality nor major complication developed. The only minor complication was wound infection which was detected in three patients. CONCLUSION: Although newer diagnostic modalities are being increasingly used to diagnose mediastinal diseases, mediastinoscopy continues to be a reliable method for the investigation of mediastinal lesions.

5.
Med Sci Monit ; 23: 3679-3686, 2017 Jul 29.
Article in English | MEDLINE | ID: mdl-28754885

ABSTRACT

BACKGROUND The lungs are the most common site of hydatid cysts in children. Rupture is the main complication of cysts causing morbidity and mortality. In this study we aimed to comprehensively describe the CT signs for cysts and analyze the relationship of cyst ruptures to the diameter and location of cyst. MATERIAL AND METHODS A total of 145 cysts from 102 patients, aged 17 years or younger, who underwent a multi-detector computed tomography (MDCT) evaluation and had surgically proven pulmonary hydatid disease were included retrospectively. The CT images were analyzed for radiologic findings and signs of cyst rupture. RESULTS The cysts had a mean diameter of 5.45±3.03 cm. Most of the patients had a solitary cyst (70.6%). The most common lobes involved were the lower lobes (58.6%). Peripherally located cysts were more common than central cysts. The overall number of ruptured cysts was 69 (47.5%). The most common sign was the waterlily sign with a prevalence of 24.6%. After exclusion of cysts of 1 cm, the mean cyst diameter was 6.23±2.83 cm in the unruptured group and 5.02±2.80 cm in the complete ruptured group (p=0.020). The mean cyst diameter was 6.38±3.11 cm for centrally located cysts, and 4.31±2.37 cm for peripherally located cysts (p<0.0001). CONCLUSIONS Pulmonary hydatid cysts commonly presents as solitary cysts with a predilection for lower lobes and the peripheral regions of the lung. Peripherally located cysts are more common but smaller than centrally located cysts. Radiologists should also be aware of atypical imaging findings of cyst rupture, and radiologic signs should be explored during radiologic evaluation.


Subject(s)
Echinococcosis, Pulmonary/complications , Echinococcosis, Pulmonary/diagnostic imaging , Adolescent , Child , Child, Preschool , Computed Tomography Angiography/methods , Echinococcosis/complications , Echinococcosis/diagnostic imaging , Female , Humans , Infant , Infant, Newborn , Lung , Male , Retrospective Studies , Rupture, Spontaneous , Tomography, X-Ray Computed/methods
6.
Medicine (Baltimore) ; 95(14): e3298, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27057899

ABSTRACT

Skeletal dysplasias are a heterogeneous group of conditions associated with various abnormalities of the skeleton. Some of them are perinatally lethal and can be diagnosed at birth. Lethality is usually due to thoracic underdevelopment and lung hypoplasia. A correct diagnosis and typing of the skeletal disorder is essential for the prognosis as is genetic counseling of the family. A retrospective review of 12 cases of clinico-radiologic diagnosis of skeletal dysplasia, leading to thoracic insufficiency, was conducted.We aimed to make differential diagnosis with special emphasis on radiological findings, and to emphasize the importance of parental counseling.


Subject(s)
Bone Diseases, Developmental/congenital , Bone Diseases, Developmental/complications , Thoracic Wall/abnormalities , Bone Diseases, Developmental/diagnostic imaging , Diagnosis, Differential , Female , Humans , Infant, Newborn , Male , Radiography , Retrospective Studies
7.
Case Rep Pulmonol ; 2015: 249612, 2015.
Article in English | MEDLINE | ID: mdl-25874150

ABSTRACT

Antiphospholipid syndrome (APS) is an autoimmune disease characterised by arterial and/or venous thrombosis and/or recurrent pregnancy loss in the presence of antiphospholipid (APL) antibodies. It is evaluated as APS when it develops associated with other systemic autoimmune diseases or primary APS if there is no concomitant disorder. In this study, we present a case of a 16-year-old male patient with primary APS. The patient was admitted with presumptive diagnosis of pneumonia, but multiple pulmonary thromboembolism (PTE) was observed on computerized tomography (CT) pulmonary angiography. APL antibodies positivity and thrombocytopenia developed in our patient. The patient was evaluated as primary APS since another etiology that could explain PTE was not found. Primary APS is a rare disease in children along with adolescents, compared with APS associated with other systemic autoimmune diseases. We present here a young male patient with primary APS and PTE to contribute to the literature. The patient initially had pneumonia but later developed PTE and thrombocytopenia.

8.
Turk J Pediatr ; 51(4): 399-402, 2009.
Article in English | MEDLINE | ID: mdl-19950855

ABSTRACT

Complex cardiovascular pathologies in the pediatric population are usually evaluated with echocardiography and catheter angiography as initial and advanced imaging of choice, respectively. Echocardiography may pose some difficulties in the diagnosis of complex cardiovascular pathologies. Due to short acquisition times, detailed imaging by the use of post-processing techniques, reduced radiation exposure compared to catheter angiography, and additional information obtained on lung parenchyma, multi-slice computed tomography (CT) is the advanced imaging method of choice in selected cases. The present report describes a 14-year-old symptomatic case with complex cardiovascular pathology, whose vascular architecture could be properly demonstrated by multi-slice CT.


Subject(s)
Aneurysm/diagnostic imaging , Aortic Coarctation/diagnostic imaging , Double Outlet Right Ventricle/diagnostic imaging , Pulmonary Artery , Tomography, X-Ray Computed/methods , Adolescent , Aneurysm/epidemiology , Aortic Coarctation/epidemiology , Double Outlet Right Ventricle/epidemiology , Heart Septal Defects, Ventricular/diagnostic imaging , Heart Septal Defects, Ventricular/epidemiology , Humans , Male , Pulmonary Artery/diagnostic imaging
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