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Port wine's prominence worldwide is unequivocal and the grape spirit, which comprises roughly one fifth of the total volume of this fortified wine, is also a contributor to the recognized quality of this beverage. Nonetheless, information about the influence of the grape spirit on the final aroma of Port wine, as well as its volatile composition, is extremely limited. Moreover, the aroma characteristics of Port wines are modulated mainly by their volatile profiles. Hence, this review presents a detailed overview of the volatile composition of the fortification spirit and Port wine, along with the methodologies employed for their characterization. Moreover, it gives a general overview of the Douro Demarcated Region (Portugal) and the relevance of fortification spirit to the production of Port wine. As far as we know, this review contains the most extensive database on the volatile composition of grape spirit and Port wine, corresponding to 23 and 208 compounds, respectively. To conclude, the global outlook and future challenges are addressed, with the position of the analytical coverage of the chemical data on volatile components discussed as crucial for the innovation centered on consumer preferences.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297353 | PMC |
http://dx.doi.org/10.3390/foods12122432 | DOI Listing |
J Am Acad Dermatol
September 2025
Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University. Electronic address:
Ann Med Surg (Lond)
September 2025
Department of Pediatrics, Faculty of Medicine, University of Aleppo, Aleppo University Hospital (AUH), Aleppo, Syria.
Introduction And Importance: To document a rare case of Sturge-Weber syndrome (SWS) Type I with acute neurological symptoms.
Case Presentation: An 11-year-old boy, previously diagnosed with Sturge-Weber syndrome (SWS) Type I, presented to the emergency department with acute neurological symptoms that included vomiting, headaches, left-sided hemiparesis, and right-sided deviation of the labial commissure.
Clinical Discussion: Sturge-Weber syndrome (SWS) is a rare neurocutaneous disorder characterized by facial port-wine stains, leptomeningeal angiomas, and ocular involvement.
Br J Dermatol
September 2025
Dermatology, Plastic and Cosmetic Surgery Center, the First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan, Guangdong, China.
Radiol Case Rep
November 2025
Department of Pediatrics and Child Health, Hawassa University College of Medicine and Health science, Hawassa, Ethiopia.
Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by a triad of clinical features: capillary malformations, venous varicosities, and hypertrophy of soft or bony tissues. This case report presents a 1-year-old infant diagnosed with KTS, exhibiting multifocal pelvic, gluteal, and thigh macrocystic lymphatic malformations alongside significant limb overgrowth. The diagnosis was confirmed through clinical evaluation and advanced imaging techniques, including Doppler ultrasound and CT angiography.
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August 2025
Department of Ophthalmology, Peking University First Hospital, Beijing, China.
Background: Sturge-Weber syndrome (SWS) is a rare congenital phacomatosis disorder. choroidal hemangioma (CH) is one of the most common ocular manifestations. The advancements in swept-source optical coherence tomography angiography (SS-OCTA) provide us a comprehensive view of the CH.
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