Hereditary elliptocytosis physical examination
Jump to navigation
Jump to search
- Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Niyousha Danesh M.D., M.P.H
Please help WikiDoc by adding content here. It's easy! Click here to learn about editing.
Overview
Physical Examination
Appearance of the Patient
- Patients are usually well-appearing in the absence of severe anemia.
- Patient appears ill in the state of septicemia.
Vital Signs
- may have Tachycardia, depends on the severity of the anemia.
- may have Tachypnea depends on severity of the anemia.
- Patients may have weak pulse
Skin
HEENT
- may have signs of meningitis due to meningococcal infection following splenectomy : neck stiffness (redor) ,fever, headache
- Evidence of trauma
- Pale conjunctiva
- Scleral icterus
Neck
No specific sign.
Lungs
- commonly normal lung sounds.
- May present crackle due to pneumococcal or Haemophilus influenza pneumonia , following splenectomy.
Heart
- commonly normal heart sounds
Abdomen
- Splenomegaly : the spleen can be palpable.
- Abdominal tenderness or fullness in the left upper quadrant following splenomegaly.
- Abdominal tenderness in the right upper quadrant due to biliary colic.
- Murphy's sign that may suggest cholecystitis.
Extremities
- Leg ulcers
Neuromuscular
- Patient is usually oriented to persons, place, and time
- Glasgow coma scale is normally 15 / 15 but may may present loss of consciousness in severe fatal hemorrhage episodes.[1][2]
References
- ↑ Barcellini W, Bianchi P, Fermo E, Imperiali FG, Marcello AP, Vercellati C; et al. (2011). "Hereditary red cell membrane defects: diagnostic and clinical aspects". Blood Transfus. 9 (3): 274–7. doi:10.2450/2011.0086-10. PMC 3136593. PMID 21251470.
- ↑ Bayhan T, Ünal Ş, Gümrük F (2016). "Hereditary Elliptocytosis with Pyropoikilocytosis". Turk J Haematol. 33 (1): 86–7. doi:10.4274/tjh.2015.0054. PMC 4805353. PMID 26377499.