Category Archives: Online

Double acute aortic syndrome in a patient with end-stage chronic kidney disease – Case report and literature review

DOI: 10.2478/amma-2026-0015

Introduction: Cardiovascular diseases are the leading cause of mortality worldwide, with aortic dissection being one of the most serious conditions, associated with high mortality. According to the Stanford classification, dissections are grouped into type A, which involves the ascending aorta and requires immediate surgery, and type B, located distal to the left subclavian artery, for which treatment may be both medical and/or endovascular. End-stage chronic kidney disease, treated by hemodialysis, is a severe risk factor owing to treatment‑resistant hypertension, vascular calcifications, and systemic fragility.
Case presentation: We present the case of a 44-year-old patient with end-stage chronic kidney disease, dependent on hemodialysis for 14 years and with hypertension refractory to treatment, with a literature review. At the first admission, the initial CT angiography revealed an extensive Stanford type B dissection with severe vascular damage for which a hybrid procedure was performed: debranching of the supra-aortic vessels, followed by thoracic endovascular repair. Two months postoperatively, due to difficult-to-control hypertension, she was readmitted for a Stanford type A dissection, requiring a redo sternotomy, replacement of the ascending aorta with a Dacron graft and revascularization of the supra-aortic branches. Despite severe comorbidities and dialysis dependence, the patient survived both interventions and was discharged in stable condition.
Conclusions: Acute aortic dissection in dialysis-dependent patients is rare but carries exceptionally high mortality. The coexistence of end-stage renal disease, refractory hypertension, and vascular calcification increases diagnostic and therapeutic challenges. Hybrid or emergency surgical–endovascular approaches can be life-saving and multidisciplinary management with careful long-term follow-up are essential to optimize prognosis.

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Persistent severe cow’s milk protein allergy on strict dietary elimination: A case report and literature review

DOI: 10.2478/amma-2026-0014

Objective: Cow’s milk protein allergy is among the most common food allergies in early childhood, yet its clinical spectrum can range from mild intolerance to life-threatening anaphylaxis. Rarely, affected children may react not only to ingestion but also to skin contact or inhalation of trace milk proteins. This report presents a detailed case of persistent and extreme hypersensitivity, illustrating the complex immunologic and psychosocial impact of the disease and highlighting the unmet need for refined preventive and therapeutic approaches.
Methods: A single pediatric case was analyzed through continuous clinical observation from infancy to seven years of age. The report integrates serial measurements of milk protein–specific immunoglobulin E, documentation of allergic reactions, dietary and environmental management, and psychosocial outcomes. The case description is complemented by a concise review of scientific literature on severe and airborne food allergies.
Results: The child exhibited immediate allergic reactions to early milk exposure and developed progressive sensitization over time, culminating in multiple anaphylactic episodes caused by minimal oral, contact, and airborne exposure. Laboratory assessments confirmed rising immunoglobulin E levels despite prolonged elimination of milk from the diet and environment. The literature review identified few comparable cases, confirming the rarity of such severe and persistent allergic phenotypes.
Conclusions: Extreme hypersensitivity to cow’s milk proteins challenges current concepts of allergy management and tolerance development. This case emphasizes the need for multidisciplinary care, structured education on anaphylaxis response, and greater community awareness to safeguard children with life-threatening food allergies.

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Intralobar pulmonary sequestration with an aneurysmal celiac arterial feeder coexisting with superior mesenteric artery syndrome: A case report and literature review

DOI: 10.2478/amma-2026-0013

Pulmonary sequestration is a rare bronchopulmonary foregut malformation characterized by the abnormal development of non-functional lung tissue enclosed by visceral pulmonary pleura, supplied by a systemic arterial blood supply, and lacking communication with the bronchial tree. The blood supply commonly arises from the thoracic or abdominal aorta. We reported a 44-year-old female who presented with vomiting and recent weight loss of about 20 kilograms in the last 6 months. The physical and biochemical examination was unremarkable. A contrast-enhanced abdominal CT scan reveals signs of superior mesenteric artery syndrome (SMAS), including a decreased aortomesenteric angle and aortomesenteric distance. The lower chest sections show an irregular consolidative lesion in the posterior segment of the Left lower lobe supplied by an aberrant aneurysmal vessel from the celiac artery, consistent with intralobar pulmonary sequestration (ILS). To our knowledge, co-occurrence of SMAS and ILS with a celiac aneurysmal feeder has not been previously reported, as both conditions affect organs of different locations and embryological origins. A literature review was conducted to examine the presentation and vascular supply of ILS.

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Conflicting pro- and anti-tumoral reports of the clock transcription factor BHLHE41 involvement in oncogenesis at the advent of spatiotemporal multiomics

DOI: 10.2478/amma-2026-0012

The bHLH-Orange transcriptional repressor BHLHE41 is considered a member of the fifth clock gene family. Diverse mechanisms of gene expression regulation and interaction with numerous transcription factors, epigenetic modifiers and master regulators often in feedback loops characterize BHLHE41 activity. BHLHE41 may be involved in oncogenesis by various mechanisms due to its pleiotropic functions. Responsive to various signals such as hypoxia or chemotherapeutics, BHLHE1 controls cell fate as a regulator of proliferation, differentiation, DNA damage repair and apoptosis. Conflicting reports of pro- and anti-tumoral effects suggest context-dependent and tumor-specific effects. BHLHE1 involvement in key mechanisms repeatedly reported include the hypoxia response and the inhibition of apoptosis and epithelial-mesenchymal transition. The sensitive balance between BHLHE41 and its paralog BHLHE40, characterized by shared and non-redundant complementary or opposing moonlighting functions, may be critical in oncogenesis. Addressing the functional complexity and heterogeneity as well as the short and long term dynamics of BHLHE41 biology by emerging spatial and temporal omics technologies may be of practical importance for precision oncology and personalized care, drug development and selection, early diagnosis and patient monitoring, or chrono-chemotherapy.

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