Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717681 | PMC |
| http://dx.doi.org/10.7860/JCDR/2015/15775.7005 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Diffuse Large B-Cell Lymphoma Presenting With Hypercalcemia.
Cureus
November 2024
Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York, USA.
Hypercalcemia is a common metabolic complication associated with malignancies, particularly in solid tumors, such as lung and breast cancers. However, its occurrence in hematologic malignancies, including diffuse large B-cell lymphoma (DLBCL), is rare. The pathophysiology of hypercalcemia in lymphomas is often related to the secretion of parathyroid hormone (PTH)-related peptide (PTHrP).
View Article and Find Full Text PDFAn Uncommon Presentation of Hamman's Syndrome in an Adolescent With Acute Diabetic Ketoacidosis and Newly Diagnosed Type 1 Diabetes.
Case Rep Pediatr
October 2024
Department of Pediatrics, Nepean Hospital, Penrith, New South Wales, Australia.
Article Synopsis
- - Hamman's syndrome is a rare complication of diabetic ketoacidosis (DKA) that causes subcutaneous emphysema and spontaneous pneumomediastinum, as demonstrated in a case involving an 11-year-old boy with newly diagnosed type 1 diabetes.
- - The patient showed classic DKA symptoms like excessive thirst, frequent urination, abdominal pain, and fatigue and was initially treated with IV fluids and insulin before being transferred to a specialized children's hospital.
- - Upon examination, he showed signs of Hamman's syndrome, which was resolved with conservative treatment, emphasizing the need for awareness of this condition in pediatric DKA cases to ensure proper diagnosis and management.
Arginine vasopressin deficiency (central diabetes insipidus) with partial empty sella: a case report.
BMC Endocr Disord
October 2024
Department of Internal Medicine, Yekatit 12 Hospital Medical College, Addis Ababa, Ethiopia.
Article Synopsis
- Arginine vasopressin deficiency leads to central diabetes insipidus, characterized by excessive urination and varying degrees of pituitary dysfunction related to a condition known as partial empty sella.
- A case study features an 18-year-old Ethiopian woman with symptoms like headaches, increased thirst and urination, and absence of menstruation, diagnosed with diabetes insipidus and a partially empty sella.
- The conclusion emphasizes the rarity of diabetes insipidus due to a partially empty sella and suggests that this condition should be considered when patients exhibit headache and pituitary dysfunction symptoms.
Beyond Vision and Hearing: A Case Report of Wolfram Syndrome.
Cureus
July 2024
Internal Medicine, Sri Ramaswamy Memorial (SRM) Medical College Hospital and Research Center, SRM Institute of Science and Technology (SRMIST), Chengalpattu, IND.
Article Synopsis
- - Wolfram syndrome (WFS) is a rare genetic disorder causing neurodegenerative symptoms like diabetes, vision and hearing loss, and various other complications.
- - A 22-year-old male with a history of type 1 diabetes developed optic nerve degeneration and sensorineural hearing loss, alongside symptoms of diabetes insipidus and polydipsia.
- - After thorough evaluation and genetic testing, he was diagnosed with WFS and is currently treated with insulin and desmopressin for his conditions.
A challenging diagnosis of Langerhans' cell histiocytosis with hypothalamic-pituitary and mandibular involvement: case report and literature review.
Ann Med Surg (Lond)
July 2024
Faculty of Medicine.
Background: Langerhans cell histiocytosis (LCH) is a rare bone marrow derived neoplasm that mainly affects children. It is a multiorgan disorder and hypothalamic-pituitary involvement is uncommon. LCH reveals a wide spectrum of indications; thus, the diagnosis and treatment are usually challenging.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!