Background/Objectives: The bifid mandibular condyle (BMC) is a rare anatomical variation characterized by a division of the mandibular condyle into two distinct heads. Although frequently identified through radiographic studies or in dry skulls, its etiology remains unclear, and few studies have examined its internal bone structure. This study aimed to perform a detailed morphologic and microarchitectural analysis of a right unilateral bifid mandibular condyle using micro-CT and to contrast the findings with the relevant morphological and clinical literature. Case Presentation: A human mandible from an anatomical collection was analyzed. The mandible was scanned using a Bruker 1273 micro-CT system, and a 3D reconstruction was performed. Morphometric analysis was carried out on both the bifid right and normal left condyles, evaluating cortical and trabecular components separately. Parameters included bone volume, absolute bone volume, bone surface, trabecular thickness, separation, and number. The right condyle was divided into medial and lateral heads with independent necks, displaying asymmetry in size and shape. Micro-CT revealed reduced cortical volume and greater trabecular separation in the BMC, suggesting lower bone density compared to the left condyle. Conclusions: This case reveals significant differences in bone architecture between the BMC and the contralateral condyle, indicating a potentially reduced biomechanical capacity on the affected side. These findings emphasize the importance of incorporating microstructural evaluation in anatomical and clinical assessments of BMCs and provide novel insights that may inform diagnosis, treatment planning, and understanding of temporomandibular joint disorders.

The updating of anatomical terms is essential to facilitate teaching and learning as well as international communication through publications and presentations at scientific events. In the posterior wall of the axilla, the teres major, teres minor and triceps brachii muscles form three spaces through which neurovascular structures of clinical significance run. The current study seeks to define and propose terms for these spaces which have been omitted by Terminologia Anatomica. The definition of the Latin term 'Spatium' was investigated using A Latin Dicionary, while the term 'Espacio' was analyzed using Diccionario panhispánico de términos médicos (Real Academia Nacional de Medicina de España, 2023), as well as the lexemes of the words 'scapula' and 'humerus', for which the Diccionario Médico-Biológico, Histórico y Etimológico de la Universidad de Salamanca was consulted. The presence of the term 'Spatium' in the Terminologia Anatomica was also investigated. Finally, 10 anatomy textbooks in Spanish were reviewed to identify the terms used for these spaces. In reviewing the latest edition of Terminologia Anatomica, it was found that the term 'Spatium' appears 25 times in different chapters and it was evident that no terms for scapulohumeral spaces appear in the chapters on upper limb structures. Moreover, in 100 % of the anatomy textbooks reviewed, at least one term is used to describe the scapulohumeral spaces. We believe that the proposed terms: 'Spatium humerotricipitale', 'Spatium scapulotricipitale' and 'Spatium teretricipitale' more accurately describe both the location and their association with the bone/muscle structures that form them. We therefore suggest that these terms be revised for inclusion in future editions of Terminologia Anatomica.

Correct detailed description of the anatomy of the digastric muscle (DM) in different populations should be carried out to improve the teaching of anatomy, avoid misinterpretations and help to avoid intercurrences during surgical procedures in the region. The aim of this study was to carry out a study of the DM in adult Brazilian individuals. The sample consisted of 50 DM from adult individuals (22 right side and 28 left side) fixed in 10 % formaldehyde. The morphology of the DM was observed, identifying possible anatomical variations; these were characterized and classified according to the number of the muscle bellies, direction of the fibre, and points of origin and insertion. The morphometric measurements were performed using a digital calliper. Student’s t-test for dependent samples was used to measure differences between sides; one-way ANOVA was used to analyse the different classifications, and the chi-squared test to analyse qualitative variables, with significance threshold of 5 %. The anterior belly of the DM was classified as Type I in 28 samples (56 %), Type II in 20 (40 %) and Type III in 2 (4 %). The mean length was 37.8 mm, width 12.1 mm and thickness 5.39 mm, with no statistically significant differences found for these variables. The intermediate tendon of the DM was classified as Type I in 31 samples (62 %), Type II in 10 (20 %) and Type III in 9 (18 %); its mean total length was 45.1 mm. The posterior belly of the DM was Type I in 50 samples (100 %), with mean length 70.8 mm and width 8.15 mm. Anatomical variations of the DM, particularly its anterior belly, in Brazilian adults are very frequent. They must therefore be carefully identified to help avoid intercurrences during surgical procedures in the region, and to help correct evaluation of swollen lymph nodes in the submental triangle.

Pediatric obesity is increasingly recognized as a biologically heterogeneous metabolic condition associated with early alterations in cardiometabolic health. Traditional clinical markers provide limited resolution for characterizing this heterogeneity, underscoring the need for more integrative approaches. Metabolomics has emerged as a powerful tool for identifying molecular phenotypes that reflect the interplay between excess adiposity, environmental and lifestyle exposures, and cardiometabolic dysfunction. This narrative review synthesizes current evidence on pediatric obesity and cardiometabolic health, with particular emphasis on metabolomic signatures, potential biological mechanisms, and early-life and lifestyle determinants. Studies using nuclear magnetic resonance spectroscopy and mass spectrometry have identified coordinated alterations in lipoprotein subclasses, triglyceride-rich particles, fatty acids and complex lipids, branched-chain and aromatic amino acids, acylcarnitines, and pathways involved in energy metabolism. These metabolic profiles are associated with insulin resistance and other adverse cardiometabolic traits. Proposed links with adipose tissue dysfunction, inflammation, mitochondrial substrate utilization, and hepatic lipid dysregulation draw partly on adult and experimental mechanistic evidence. Early-life and lifestyle exposures, including maternal health, infant feeding, dietary patterns, physical activity, sleep, and environmental factors, may further shape these metabolic phenotypes. Integrating metabolomic information with clinical and environmental data may improve the characterization of metabolic heterogeneity and help identify biological pathways associated with early cardiometabolic dysfunction. However, classification of current metabolic phenotypes does not establish prediction of future disease. Independent prospective validation, methodological harmonization, and demonstration of incremental clinical utility remain necessary before metabolomic profiling can be incorporated into routine pediatric risk assessment.