Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis (1464 page)

BOOK: Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis
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MCV
hemoglobin D (HbD) disease
Hb variant
spherocytes
hemoglobin E (HbE) disease
β-thalassemia disease
CBC
Hb variant
microcytes
hemoglobin H disease
hereditary spherocytosis
myeloproliferative neoplasms
polycythemia vera
ulcerative colitis, chronic nonspecific
variant analysis
alpha thalassemia syndromes
β-thalassemia major
β-thalassemia minor
HbC
HbD disease
HbE disease
hemoglobinopathies
hereditary elliptocytosis
sickle cell disease
sickle cell screen

Hemoglobin A1c (HbA1c)

diabetes and vasculopathies
diabetes mellitus
diabetic nephropathy

Hemoglobinopathies

hemoglobin S–hemoglobin C disease
hemoglobin variant analysis
mean corpuscular volume
reptilase time
sickle cell disease
See
(Sickle cell disease (SCD))

Hemoglobinuria

antiglobulin test
conjugated bilirubin
Coombs test
haptoglobin
hematuria
hemolytic anemias with intravascular hemolysis
limitations
serum LDH
urine urobilinogen

Hemolysis

Hemolytic anemias

autoimmune
diabetes mellitus
with intravascular hemolysis, hemoglobinuria
parvovirus B19

Hemolytic complement activity (CH50)

postinfectious GN

Hemolytic disease of the fetus and newborn (HDFN)

agglutination
DAT

Hemolytic extrinsic red blood cell defects

AIHAs anemias
Evans syndrome
hemolytic disease, in newborn
mechanical hemolytic anemias
PCH anemia
PNH disorder

Hemolytic intrinsic red blood cell defects

G6PD deficiency
HE disorder
hereditary stomatocytosis
HO disorder
HP disorder
HS disorder
PK deficiency

Hemolytic transfusion reactions (HTR)

agglutination

Hemolytic uremic syndrome (HUS)

Escherichia coli
plasma transfusion
platelet count
spectrum of

Hemophilia

factor IX (F IX) deficiency
factor VIII (F VIII) deficiency
factor XI (F XI) deficiency
factor XII (F XII) deficiency
factor XIII (F XIII) deficiency
von Willebrand disease (VWD)

Hemophilia A

acquired anti-factor VIII
anticoagulants
factor VIII
lymphoma
PTT

Hemophilia B

anticoagulants
factor VIII
lymphoma
PTT

Hemorrhage

neutrophilia
SIADH

Hemorrhagic disorders, acquired, multifactorial etiology

circulating anticoagulants
coagulopathy of liver disease
disseminated intravascular coagulation
hemostatic failure in cardiopulmonary bypass surgery
hereditary hemorrhagic telangiectasia

Hemosiderin, mechanical hemolysis

Hemostatic failure

in cardiopulmonary bypass surgery
D
-dimer
DIC
thromboelastogram

Henoch–Schönlein purpura (HSP)

BUN
creatinine
GFR
IgA nephropathy
nephritic syndrome
nephritis

Heochromocytoma, systolic dysfunction with heart failure

Heparan sulfatase deficiency.
See
Sanfilippo type A syndrome

Heparin

Heparin anti-Xa (Low molecular weight heparin)

Heparin-induced platelet aggregation

Heparin-induced thrombocytopenia (HIT)

assays
clinical diagnosis
DIC
thrombophilia

Hepatic transaminase, hyperbilirubinemia

Hepatitis

acute phase
albumin levels
ALP
ALT
AST
CBC
cholesterol
ESR
iron
LD
protein electrophoresis
PT
ALT
ameba
AST
autoimmune
CMV
disease manifestation
EBV-rubella
enteric routes, HAV
fulminant
hepatitis A IgM antibody
hepatitis A virus (HAV)
hepatitis B core IgM antibody
hepatitis B surface antigen
hepatitis B virus (HBV)
hepatitis C antibody
hepatitis C virus (HCV)
hepatitis D virus (HDV)
hepatitis E virus (HEV)
hepatocellular carcinoma
IgM anti-HAV
IgM anti-HBc
laboratory overview
leishmania
M. tuberculosis
postacute phase
prodromal phase
total anti-HBc
total anti-HVC
transmission
by blood-borne routes
by enteric routes
types of

Hepatitis A virus (HAV)

antibodies
anti-HAV-IgM
GI symptoms
hepatitis viruses, enteric routes

IgM antibody

Hepatitis B virus (HBV)

acute HBV infection
ALT
anti-HBc
anti-HBc antibodies
anti-HBc IgM
anti-HBc total
anti-HBc-IgG
anti-HBe
anti-HBs
BE antigen and antibody
core antibodies
core antigens
core IgM antibody
cryoglobulinemia
DNA
acute HBV infection with recovery
by PCR
HBcAb
HBeAg
HBsAb
HBsAg
HBV/HDV coinfection
hepatitis B core antigens
hepatitis B e-antigen (HBeAg)
acute liver failure
chronic HBV infection
HBV
negative, HBV
human immunodeficiency virus
IgM antibodies
hepatitis B surface antigen
acute liver failure (ALF)
cholangitis, primary sclerosing
negative, HBV
positive, chronic HBV infection
during pregnancy
surface antibody

Hepatitis C virus (HCV)

AFP
alkaline phosphatase
ALT
antibody
antigen
bilirubin
CBC
complement system
genotype
genotyping assay
HCV viral loads
HDL
human immunodeficiency virus (HIV)
25-hydroxy-vitamin D3 level
ITP
LDL
PT
RIBA
RNA
spontaneous coronary artery dissection
Triglyceride
viral load assay

Hepatitis D virus (HDV)

antibody
anti-HBc-IgG
anti-HBc-IgM
anti-HDV
anti-HDV-IgM
anti-HDV-total
HBsAg
HBV/HDV coinfection
HDAg
IgM anti-HDV
RNA

Hepatitis E virus (HEV)

antibody
anti-HEV-IgG
anti-HEV-IgM
GI symptoms
BOOK: Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis
12.81Mb size Format: txt, pdf, ePub
ads

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