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Short Communication | Open Access
Published on: 07 Feb 2026
Article ID: wjed.2026.b0705
Acromegaly and Hirsutism: Exploring a Rare Association
Introduction
Acromegaly is a rare endocrine disorder caused by excessive secretion of Growth Hormone (GH), usually from a pituitary adenoma [1]. Hirsutism, a condition characterized by excessive terminal hair growth in a male pattern in women, has been occasionally reported as a cutaneous manifestation of acromegaly but is rarely the presenting symptom [2, 3]. We report a rare case of acromegaly revealed by hirsutism.
Mini Review | Open Access
Published on: 07 Feb 2026
Article ID: wjhp.2026.b0707
Nursing Management of Acute Liver Failure: A Clinical Review
Acute Liver Failure (ALF) is a rapid and severe clinical syndrome defined by the onset of liver dysfunction and encephalopathy within eight weeks of symptoms in healthy individuals, or two weeks following jaundice in those with pre-existing disease. ALF arises from diverse etiologies. Nursing management is a cornerstone of ALF care, requiring intensive monitoring of neurological status, hemodynamic stability, and fluid-electrolyte balance. Specific interventions include managing cerebral…
Review Article | Open Access
Published on: 07 Feb 2026
Article ID: wjnr.2026.b0708
Comprehensive Nursing Guide to Osteoporosis Management
Osteoporosis is a "silent disease" characterized by reduced bone mass and increased skeletal fragility, making nurses' roles in education, prevention as well as holistic support, critical. Key nursing interventions focus on lifestyle modifications, fall prevention strategies, coordination of pharmacological therapy and psychosocial support. By promoting early screening, nurses can significantly reduce the morbidity and mortality associated with osteoporotic fractures. Specialized nursing…
Perspective | Open Access
Published on: 07 Feb 2026
Article ID: wjms.2026.b0709
Artificial Intelligence in Pain Management
Perspective Artificial intelligence (AI) has rapidly emerged as a transformative force in modern healthcare, enabling data-driven approaches to diagnosis, treatment planning, and clinical decision-making [1]. By incorporating techniques such as machine learning, deep learning, data mining, and natural language processing, AI systems are increasingly capable of analyzing complex clinical data and supporting personalized care [2]. One area that has recently gained attention is…
Opinion | Open Access
Published on: 07 Feb 2026
Article ID: wjptr.2026.b0710
An Analysis of Soleus Muscle Tightness and Intrinsic Foot Muscle Weakness in Individuals with Flatfoot – A Cross Sectional Study
Background: Flat foot is related with modified foot biomechanics, where intrinsic foot muscle weakness and calf muscle tightness, particularly of the soleus muscle are deemed assisting factors. Understanding the relationship between these variables may and in better assessment and rehabilitation strategies for individuals with flatfoot.
Objective: To analyze the relationship between intrinsic foot muscle strength, soleus muscle tightness in…
Mini Review | Open Access
Published on: 07 Feb 2026
Article ID: wjat.2026.b0711
Cancer as an Anatomical Disease
Cancer is most commonly described as a molecular and genetic disorder driven by mutations that alter cell proliferation and survival. However, malignant transformation also represents an anatomical phenomenon characterized by progressive disruption of normal tissue architecture at cellular, histological, and organ levels. This brief review examines cancer from an anatomical perspective, emphasizing alterations in tissue organization, cellular morphology, stromal composition, vascular…
Case Report | Open Access
Published on: 02 Feb 2026
Article ID: wja.2026.b0201
A Rare Constellation of Multiple Allergies, Chronic Urticaria, Micronutrient Deficiencies, and Multisystem Manifestations of Colorectal Motility Disorder in a Teenage Girl
Multisystem presentations in adolescents often lead clinicians down fragmented diagnostic pathways. Chronic urticaria, multiple allergies, and micronutrient deficiencies are typically approached through immunological or nutritional frameworks, while gastrointestinal dysmotility is often siloed within gastroenterology. This case highlights the diagnostic complexity and systemic interplay between immune dysregulation, nutritional compromise, and colorectal motility disorder in a teenage girl…
Research Article | Open Access
Published on: 02 Feb 2026
Article ID: wjacs.2026.b0202
Institutional Challenges and Governance Pathways for Agricultural Cultural Heritage Conservation in Hebei Province
As a major agricultural province, Hebei boasts abundant agricultural cultural heritage resources, currently housing 3 globally important agricultural cultural heritage sites and 5 nationally important ones in China. This paper conducts an in-depth analysis of the current operational status of the agricultural cultural heritage system in Hebei, identifying such issues as the absence and fragmentation of institutional content, impeded implementation mechanisms coupled with a lack of…
Review Article | Open Access
Published on: 31 Jan 2026
Article ID: wjem.2026.a3101
The Burning Global Issues in Emergency Medicine: A Narrative Review
Objectives: To synthesise and critically examine the most urgent global challenges facing Emergency Medicine (EM), including system pressures, workforce vulnerabilities, climate‑related threats, conflict‑driven emergencies, infectious disease risks, inequities in access, and gaps in digital and research capacity. The review aims to identify cross‑cutting determinants and propose system‑level strategies to strengthen resilience and equity in emergency care…
Case Report | Open Access
Published on: 31 Jan 2026
Article ID: wjo.2026.a3102
Familial Metachronous Wilms’ Tumour in a Sibling with Previous Bilateral Synchronous Wilms’ Tumour: A Rare Familial Cluster
Wilms Tumour (WT) is the most common renal malignancy of childhood, typically occurring sporadically. Familial WT accounts for fewer than 2% of cases and often involves germline predisposition syndromes. Metachronous WT in siblings - particularly when one sibling previously presented with bilateral synchronous disease - is exceptionally rare. We report a case of a child presenting with unilateral WT whose older sibling had been treated several years earlier for bilateral synchronous WT. This…
DOI: 10.5281/zenodo.18778451 »