NASCI case of the month: 'Intramyocardial dissecting hematoma'.

Intramyocardial dissecting hematoma (IDH) usually develops from hypoxia-induced capillary destruction within the myocardium following ischemia. The hematoma then infiltrates the interstices between myocardial spiral fibers, establishing a neocavity. As intra-neocavitary pressure increases, the hematoma expands and occasionally becomes associated with the epicardium or ventricular cavity (Roslan A et al. (2017) Intramyocardial dissecting hematoma in patients with ischemic cardiomyopathy: role of multimodality imaging in three patients treated conservatively. CASE: Cardiovasc Imaging Case Rep 1(4):159). Differential diagnoses include prominent ventricular trabeculations, intracavitary thrombosis, and pseudoaneurysm. By confirming the integrity of the epicardium, IDH can be distinguished from pseudoaneurysm, characterized by a complete rupture of the myocardial wall enclosed by the pericardium. Clear identification of the endocardium surrounding the hematoma and its systolic expansion may help to differentiate IDH from intracavitary hematoma. Prominent trabeculations can be recognized by a ventricular wall with an utterly asymmetric flow pattern (Vasco Dias (June 2009) et al., Intramyocardial dissecting haematoma: a rare complication of acute myocardial infarction. Eur J Echocardiography 10(4):585-587).

The Thyroidea Ima Artery Arising from the Aortic Arch: A Rare Anatomical Variation.

A 73-year-old man underwent computed tomography (CT) angiography assessment of the head and neck vasculature. An incidental note of the thyroidea ima artery arising from the aortic arch was made. Presence of thyroidea ima artery may have clinical importance prior to neck surgeries and minimally invasive interventions.

Dual origin of the left vertebral artery: a rare anatomic variation.

Duplication of the vertebral artery is a very rare vascular variant. We describe a case of a duplicated left vertebral artery. Computed tomography (CT) angiography examination of the head and neck vessels of a 63-year-old man with a history of imbalance was undertaken. A duplicated left vertebral artery was incidentally noted. The medial limb directly originated from the arcus aorta between the left common carotid artery and the left subclavian artery. The lateral limb originated from the proximal left subclavian artery as the first branch and entered the transverse foramen of the C6 vertebra as usual. Prior to neck procedures requiring the anterior cervical approach and carotid endarterectomy, the awareness and diagnosis of the duplicated vertebral artery are important due to the potential risk of inadvertent vertebral artery injury. Therefore, this variation should be taken into account while evaluating cross-sectional imaging studies.

Splenic Gaucheroma Leading to Incidental Diagnosis of Gaucher Disease in a 46-Year-Old Man with a Rare GBA Mutation: A Case Report.

BACKGROUND: Gaucher disease is a common lysosomal storage disease caused by the deficiency of the ß-glucosidase enzyme, leading to sphingolipid accumulation in the reticuloendothelial system in Gaucher cells. Clinical findings are quite variable and some patients may remain asymptomatic lifelong. However, even when patients have mild symptoms, there is a significant increase in their quality of life with enzyme replacement therapy. We aimed to reveal the relationship between a rare mutation in the Glucosylceramidase Beta (GBA) gene and clinical signs and symptoms. Another aim of the study was to show the effect of enzyme replacement therapy on the quality of life, even in patients with mild symptoms. CASE PRESENTATION: Here, we report a 46-year-old male diagnosed with Gaucher disease based on splenic Gaucheromas incidentally discovered in a cardiac computerized tomography scan. In GBA gene analysis, the extremely rare R87W mutation was detected in a homozygous state. In retrospect, the patient had nonspecific symptoms such as fatigue and bone pain for a long time, which were substantially ameliorated by enzyme replacement therapy. CONCLUSION: In patients with adult-onset Gaucher disease, the symptoms may be mild, causing significant diagnostic delay. Gaucher disease may be included in the differential diagnosis of abdominal malignancies. Early diagnosis and treatment can improve quality of life and prevent unnecessary procedures.

Approach to optimal assessment of right ventricular remodelling in heart transplant recipients: insights from myocardial work index, T1 mapping, and endomyocardial biopsy.

AIMS: Right ventricular (RV) dysfunction is an important cause of graft failure after heart transplantation (HTx). We sought to investigate relative merits of echocardiographic tools and cardiac magnetic resonance (CMR) with T1 mapping for the assessment of functional adaptation and remodelling of the RV in HTx recipients. METHODS AND RESULTS: Sixty-one complete data set of echocardiography, CMR, right heart catheterization, and biopsy were obtained. Myocardial work index (MWI) was quantified by integrating longitudinal strain (LS) with invasively measured pulmonary artery pressure. CMR derived RV volumes, T1 time, and extracellular volume (ECV) were quantified. Endomyocardial biopsy findings were used as the reference standard for myocardial microstructural changes. In HTx recipients who never had a previous allograft rejection, longitudinal function parameters were lower than healthy organ donors, while ejection fraction (EF) (52.0 ± 8.7%) and MWI (403.2 ± 77.2 mmHg%) were preserved. Rejection was characterized by significantly reduced LS, MWI, longer T1 time, and increased ECV that improved after recovery, whereas RV volumes and EF did not change MWI was the strongest determinant of rejection related myocardial damage (area under curve: 0.812, P < 0.0001, 95% CI: 0.69-0.94) with good specificity (77%), albeit modest sensitivity. In contrast, T1 time and ECV were sensitive (84%, both) but not specific to detect subclinical RV damage. CONCLUSION: Subclinical adaptive RV remodelling is characterized by preserved RV EF despite longitudinal function abnormalities, except for MWI. While ultrastructural damage is reflected by MWI, ECV, and T1 time, only MWI has the capability to discriminate functional adaptation from transition to subclinical structural damage.

Nerves of the Thorax: Anatomy, Clinical Signs, and Imaging Findings of Pathological Conditions.

BACKGROUND: Radiological diagnosis of thoracic nerve diseases is difficult because they are rare, and nerves cannot be seen directly on radiological images. The major nerves of the thorax can be listed as the phrenic, vagus, recurrent laryngeal, long thoracic nerve pairs, sympathetic chains, costal nerves, and brachial plexus. Diseases of thoracic nerves have various causes, including traumatic injury, neuromuscular diseases, infection, compression, radiation, drugs, and tumors. OBJECTIVE: This pictorial review aims to describe the anatomic locations of the major thoracic nerves on radiological images, comprehensively describe the causes of thoracic nerve diseases and define the clinical signs and primary and secondary imaging findings of dysfunction of the thoracic nerves. METHODS: This paper was designed to illustrate primary and secondary imaging findings of nerve diseases. Firstly, the normal anatomy of nerves is shown with diagrams. Secondly, we explained primary and secondary imaging features with variable radiological methods, including chest X-Ray, magnetic resonance imaging, and computed tomography. CONCLUSION: Primary findings of nerve diseases can be detected if radiologists are familiar with the courses of the nerves on radiological images. Knowledge of the normal functions of the nerves can aid in diagnosing thoracic nerve diseases identified from secondary imaging findings such as diaphragmatic elevation, muscular atrophy, and winged scapula. It is essential to know the normal anatomy, function, and possible causes of thoracic nerve diseases to make a correct diagnosis and apply the prompt treatment.

COVID-19 pneumonia: the great radiological mimicker.

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has rapidly spread worldwide since December 2019. Although the reference diagnostic test is a real-time reverse transcription-polymerase chain reaction (RT-PCR), chest-computed tomography (CT) has been frequently used in diagnosis because of the low sensitivity rates of RT-PCR. CT findings of COVID-19 are well described in the literature and include predominantly peripheral, bilateral ground-glass opacities (GGOs), combination of GGOs with consolidations, and/or septal thickening creating a "crazy-paving" pattern. Longitudinal changes of typical CT findings and less reported findings (air bronchograms, CT halo sign, and reverse halo sign) may mimic a wide range of lung pathologies radiologically. Moreover, accompanying and underlying lung abnormalities may interfere with the CT findings of COVID-19 pneumonia. The diseases that COVID-19 pneumonia may mimic can be broadly classified as infectious or non-infectious diseases (pulmonary edema, hemorrhage, neoplasms, organizing pneumonia, pulmonary alveolar proteinosis, sarcoidosis, pulmonary infarction, interstitial lung diseases, and aspiration pneumonia). We summarize the imaging findings of COVID-19 and the aforementioned lung pathologies that COVID-19 pneumonia may mimic. We also discuss the features that may aid in the differential diagnosis, as the disease continues to spread and will be one of our main differential diagnoses some time more.

Radiological manifestations of thoracic hydatid cysts: pulmonary and extrapulmonary findings.

Hydatid cyst caused by the larval form of Echinococcus is a worldwide zoonosis. The lungs and liver are the most common sites involved. While the lung parenchyma is the most common site within the thorax, it may develop in any extrapulmonary region including the pleural cavity, fissures, mediastinum, heart, vascular structures, chest wall, and diaphragm. Imaging plays a pivotal role not only in the diagnosis of hydatid cyst, but also in the visualization of the extent of involvement and complications. The aim of this pictorial review was to comprehensively describe the imaging findings of thoracic hydatid cyst including pulmonary and very unusual extrapulmonary involvements. An outline is also given for the findings of complications and differential diagnosis of thoracic hydatid cyst.