Wednesday, September 16, 2026
Shoulder with Details of Glenohumeral Joint Anatomy
Shoulder with Details
of Glenohumeral Joint Anatomy
Anterior view, Acromion, Coracoacromial
ligament, Supraspinatus tendon (cut), Coracohumeral ligament, Greater
tubercle, Transverse humeral ligament, Intertubercular tendon sheath (communicates
with synovial cavity), Acromioclavicular joint capsule (incorporating
acromioclavicular ligament), Subscapularis tendon (cut), Biceps brachii
tendon (long head), Clavicle, Trapezoid ligament Coracoclavicular, Conoid
ligament ligament, Superior transverse scapular ligament and superior scapular (suprascapular)
notch, Coracoid process, Opening of subtendinous bursa of subscapularis muscle,
Tuesday, September 15, 2026
Monday, September 14, 2026
Diagnosis of Death: Circulatory Death, Brainstem Death, and Physiology
Diagnosis
Of Death And Its Physiology
Diagnosing death
Circulatory death
Traditionally, death has been certified by the absence of a circulation,
usually taken as the point at which the heart stops beating. In the UK, current
guidance suggests that death may be confirmed after 5 minutes of observation
following cessation of cardiac function (e.g. absence of heart sounds, absence
of palpable central pulse or asystole on a continuous electrocardiogram). Organ
donation after circulatory death (DCD) may occur following confirmation that
death has occurred (also called non-heart-beating donation). There are two sorts of DCD donation, controlled and uncontrolled.
Thursday, September 10, 2026
Myxedema: Symptoms, Causes, Skin Findings, Diagnosis & Treatment
MYXEDEMA
Myxedema is seen in patients with untreated severe
hypothyroidism. This condition results from a total lack of thyroid hormone
secretion and resultant deposition of mucopolysaccharides into the skin and
other organs. Many skin and systemic findings are present in severe
hypothyroidism. This is a condition seen in adults. The infantile form, called
cretinism, is still found in parts of the world that do not routinely test
newborn infants. If it is left untreated, mental retardation and various
neurological deficits can occur. Adult myxedema is an uncommon clinical
disease.
Wednesday, September 9, 2026
Cross Section at L3–4 Anatomy
Cross Section at L3–4 Anatomy
Round ligament (ligamentum teres) of liver, Transverse colon, Branches of inferior
epigastric vessels, Rectus sheath, Transversus abdominis aponeurosis, External oblique aponeurosis, Internal oblique
aponeurosis, Mesentery
of small intestine, Superior mesenteric vessels, Small intestine (ileum),
Lymph node, Ascending colon, Right paracolic gutter, Tendon of origin of transversus abdominis muscle, Ilioinguinal nerve,
Tuesday, September 8, 2026
Dermatomyositis: Symptoms, Causes, Diagnosis, Histology & Treatment
Dermatomyositis
Dermatomyositis is a chronic
connective tissue disease that can be associated with an underlying internal
malignancy. This connective tissue disease shares similarities with
polymyositis, but the latter has no cutaneous findings. Up to one third of
patients with dermatomyositis have an underlying malignancy. The myositis is
often prominent and manifests as tenderness and weakness of the proximal muscle
groups. The pelvic and shoulder girdle muscles are the ones most commonly
affected. Dermatomyositis sine myositis is a well-recognized variant that has
only the cutaneous findings; evidence of muscle involvement is absent.
Monday, September 7, 2026
Topography and Constrictions of Esophagus Anatomy
Topography and Constrictions of Esophagus Anatomy
Incisor tooth, Oropharynx, Epiglottis, Piriform recess, Thyroid cartilage, Cricoid cartilage, Thyroid cartilage, Cricoid cartilage, Cricopharyngeus (muscle) part of inferior pharyngeal constrictor muscle, Pharyngoesophageal constriction, Average
length in centimeters, Thoracic (aortobronchial) constriction, Trachea, Arch of aorta, Left main bronchus,
Alport Syndrome and Thin Basement Membrane Nephropathy: Causes, Symptoms, Diagnosis & Treatment
HEREDITARY
NEPHRITIS (ALPORT SYNDROME)/THIN
BASEMENT MEMBRANE NEPHROPATHY
Hereditary nephritis (HN, also known as Alport
syndrome) and thin basement membrane nephropathy (TBMN) are both inherited
disorders that feature structural defects in type IV collagen, an integral
component of the glomerular basement membrane. Both conditions present in
childhood with persistent microscopic hematuria.
HN is rare, affecting 1 in 50,000
individuals, and often progresses to end stage renal disease (ESRD). TBMN, in
contrast, affects 1 in 20 to 100 individuals and typically does not have a
progressive course.
Sunday, September 6, 2026
Intracellular Accumulations: Causes, Types, Examples, and Clinical Significance
Intracellular accumulations
represent the buildup of substances that cells cannot immediately use or
eliminate. The substances may accumulate in the cytoplasm (frequently in the
lysosomes) or in the nucleus. In some cases the accumulation may be an abnormal
substance that the cell has produced, and in other cases the cell may be
storing exogenous materials or products of pathologic processes occurring
elsewhere in the body. An example would be the accumulation of beta amyloid
fragments, which progress to a skeletal muscle disorder called myositis. These
substances may accumulate transiently
or permanently, and they may be
harmless or, in some cases, toxic.









