2. Length – approx 12cm (5 inches) in adults
Weight – approx 160 g
Colour – deep red
Position
◦ Between 9th
to 11th
ribs on left side
3. ◦ Splenic artery
From coeliac trunk (T12), a branch of the abdominal aorta
Branches into trabecular arteries
Further branches surrounded by white pulp
Capillaries discharge blood into red pulp
◦ Splenic vein
Joins SMV to form hepatic portal vein
4. Gastrosplenic ligament
◦ Broad band of mesentery
◦ Attaches spleen to lateral border of stomach
Surfaces
◦ Diaphragmatic – smooth and convex
◦ Visceral – i.e. conforming to shape of:
Stomach (gastric area)
Left kidney (renal area)
Hilum
◦ Pt of communication of splenic vessels with spleen
◦ Groove that marks border between gastric and renal
areas.
5.
6. Surrounding capsule – collagen + elastic fibres
Cellular components divided into ‘pulp’:
Red pulp •Function – mechanical filtration of RBCs
•Contains – RBCs, blood components, free and fixed
macrophages
•Sequence of filtration – network of reticular fibres
blood-filled sinusoids lined with macrophages small
veins trabecular veins hilum
•NB: marginal zone i.e. where red pulp meets white
White pulp •Function – active immune response via humoral and
cell-mediated pathways.
•Composed of nodules (Malpighian corpuscles):
•Lymphoid follicles – rich in B cells
•Periarteriolar lymphoid sheathes (PALS) – rich in T
cells
7. 1. Removal of abnormal RBCs and other
blood components (via phagocytosis)
2. Fe storage (recycled from RBCs)
3. Initiation of immune responses by B
and T cells in response to circulating
antigens
8. Cannot get above it (ribs overlie the top)
Dull to percussion (kidneys are resonant due to
underlying bowel)
Moves more with inspiration towards RIF
Medial notch
9. Causes can be divided into:
◦ Infective
◦ Haematological
◦ Neoplastic
Also can be grouped with associated features
◦ Fever
◦ Lymphadenopathy
◦ Purpura
◦ Arthritis
◦ Ascites
◦ Murmurs
◦ Anaemia
◦ Weight loss and CNS signs
◦ Massive
Sjogren’s syndrome
Systemic autoimmune disease that targets exocrine glands producing tears and saliva.
Dry mouth (xerostomia) and dry eyes (xeropthalmia)
Lyme disease
Borellia (genus of bacterium)
Transmitted by ticks
Symptoms – early: fever, headache, fatigue, erythema migrans. Later – joints, heart, CNS symptoms.
Treated with Abx
Behcet’s
Immune-mediated systemic vasculitis
Mucous membrane ulceration and ocular involvements
Triad
Recurrent oral aphthous ulcers
Genital ulcers
Uveitis
Leishmaniasis
Leishmania (protozoan parasites)
Transmitted by sandflies
Cutaneous skin sores
Pernicious anaemia
Usually from autoimmune destruction of gastric parietal cells
Resultant lack of intrinsic factor, IF
Poor B12 absorption from the gut
B12 deficiency anaemia
POEM (Polyneuropathy, Organomegaly, Endocrinopathy, M-protein band)
Also associated with hypothyroidism
Gaucher’s disease:
Most common lysosomal storage disease
Hereditary deficiency of enzyme glucosylceramidase which acts on FA glucosylceramide.
AR mutation in chromosome 1
Higher rates in Ashkenazi Jews (also prone to HNPCC, haemophilia C, Parkinson’, Crohn’s, familial hypercholesterolaemia, familial hyperinsulinaemia etc.)
Lipid accumulation in cells and organs
Especially in WBCs i.e. macrophages
Collect in spleen, liver, kidneys, lungs, brain, bone marrow
Symptoms
Hepatosplenomegaly
Liver malfunction
Skeletal disorders and bone lesions
Neurologic complications
Lymphadenopathy
Brownish tint to skin
Anaemia
Neutropenia
Jaundiced sclera
Increased susceptibility to infection