This case presentation describes a 55-year-old male referred for management of severe anemia. He has a history of recurrent kidney stones, hypertension, diabetes, and back pain. Laboratory tests reveal severe anemia with rouleaux formation. Further workup shows evidence of a gammopathy. A bone marrow biopsy is needed to confirm a diagnosis of multiple myeloma, which can cause anemia and kidney damage through paraprotein production and bone lesions. Treatment involves supportive care, chemotherapy, and stem cell transplantation in eligible patients.
This document provides an overview of anemia, including its classification, causes, signs and symptoms, diagnostic approach, and management principles. It presents a clinical case of an 18-year-old female with weakness, lethargy and heavy menstrual bleeding, then reviews epidemiology of anemia, the red blood cell lifecycle, classification of anemia by severity, etiology and morphology, diagnostic workup, and general management strategies focusing on identifying and treating underlying causes. The take-home message emphasizes that anemia requires investigation to determine its cause, and prevention through supplementation is important for reducing prevalence.
This document provides guidance on evaluating and managing anemia in patients. It discusses evaluating the cause of anemia based on history, physical exam, and lab tests. Causes in critically ill patients especially include blood loss from phlebotomy and bleeding, decreased erythropoiesis from inflammation, and nutritional deficiencies. Transfusions are used to manage anemia but have risks, so restrictive protocols targeting Hgb <7g/dL are recommended except for patients with cardiovascular conditions. New blood substitutes are still experimental and have shown adverse effects.
1) Pancytopenia refers to decreases in all peripheral blood cell lines, specifically red blood cells, white blood cells, and platelets. Common causes include bone marrow infiltration, aplasia, or blood cell destruction.
2) Evaluation of pancytopenia involves a thorough history and physical exam focusing on symptoms, exposures, medications, and signs of organomegaly or lymphadenopathy.
3) Initial laboratory tests include a complete blood count, blood smear, and basic metabolic panel. Additional tests may include coagulation studies, blood cultures, serologies, and bone marrow examination based on specific clinical or laboratory findings.
Chronic liver disease in children22.pptxAmmaraHameed6
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This document discusses chronic liver disease and portal hypertension in children. It defines chronic liver disease as ongoing liver injury for at least 6 months that can progress to cirrhosis and liver failure. Cirrhosis is the end result of liver cell damage and destruction. The etiology of chronic liver disease in children varies according to age and includes infectious, metabolic, autoimmune, anatomical, and toxic/drug-induced causes. Some common chronic liver diseases in children discussed in detail include biliary atresia, alpha-1 antitrypsin deficiency, cystic fibrosis, and Wilson's disease.
The document discusses proteinuria and hematuria in children. It covers the definition, causes, evaluation, and treatment of both conditions. Proteinuria can be caused by glomerular, tubular, or overflow mechanisms and is evaluated through urine dipsticks, 24-hour urine collection, and urine protein to creatinine ratio. Hematuria can be gross or microscopic and is seen in conditions like UTI, nephrolithiasis, glomerulonephritis, IgA nephropathy, and Alport syndrome. Evaluation of hematuria involves urinalysis, urine culture, imaging, and considering familial causes. Specific renal diseases like post-streptococcal glomerulonephritis
This patient with newly diagnosed myeloma presented with a large gluteal hematoma one week following a bone marrow biopsy. Initial workup found decreased factor XIII antigen and activity levels. Further testing showed evidence of amyloid deposits on fat pad biopsy and cardiac MRI consistent with amyloidosis, which can cause acquired bleeding disorders through effects on coagulation factors and platelets. The differential diagnosis includes evaluating for qualitative or quantitative platelet disorders, coagulation factor deficiencies, and structural causes of bleeding in the setting of a paraproteinemia like myeloma.
1) An 85-year-old woman was hospitalized for severe anemia with a hemoglobin of 3 g/dL.
2) A 76-year-old man seen for forgetfulness and difficulty walking was found to have peripheral neuropathy and anemia with hypersegmented neutrophils on blood smear.
3) A 16-year-old female with autoimmune hepatitis developed anemia with heavier menses and petechiae; bone marrow showed mild dyserythropoiesis and hypocellularity.
Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by blood clots in arteries and veins, pregnancy complications, and the presence of antiphospholipid antibodies. The condition occurs when the immune system produces antibodies that cause blood to clot abnormally. Treatment involves blood thinners and aspirin to prevent clots, with lifelong anticoagulation often needed for recurrent clotting events. Prognosis depends on symptom severity and control, with catastrophic APS having high mortality without aggressive intervention.
This document provides information about tumor lysis syndrome (TLS), including its definition, risk factors, pathophysiology, and management. TLS is an oncometabolic emergency that can occur after tumor targeted therapy leads to rapid cell death and release of cellular contents like uric acid, potassium, and phosphorus. It can cause abnormalities in electrolytes and kidney injury. High risk groups include those with hematologic malignancies like lymphoma. Management involves prevention, monitoring, volume expansion, and in some cases urinary alkalinization or allopurinol.
1. Chronic cholestasis can be caused by intrahepatic or extrahepatic conditions. Common intrahepatic causes include primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), and drug-induced liver injury (DILI).
2. PBC is an autoimmune disease characterized by progressive destruction of intrahepatic bile ducts, presence of antimitochondrial antibodies (AMA), and histologic findings of florid duct lesions on liver biopsy. PBC diagnosis requires two of three criteria: cholestatic liver enzymes, AMA positivity, or liver biopsy consistent with PBC.
3. PSC is a chronic inflammatory condition of
This document provides information on several gastrointestinal conditions:
1. Achalasia is a motility disorder of the esophagus characterized by loss of peristalsis and failure of the lower esophageal sphincter to relax properly.
2. Esophageal cancer can be squamous cell carcinoma or adenocarcinoma, with risk factors including smoking, alcohol, and Barrett's esophagus. Treatment depends on cancer stage and may include surgery, chemotherapy, or radiation.
3. Peptic ulcer disease is caused by a bacterial infection with H. pylori in most cases. Treatment involves eradicating H. pylori with antibiotic therapy and proton pump inhibitors.
The document discusses antiphospholipid syndrome (APS), a condition characterized by abnormal blood clotting caused by antibodies against phospholipids. It outlines the criteria for diagnosis, including recurrent blood clots or pregnancy loss alongside persistent antiphospholipid antibodies. Management involves long-term anticoagulation for clots and aspirin with heparin during pregnancy to prevent complications. A rare but severe form called catastrophic APS can affect multiple organs and requires aggressive treatment.
Hematuria, or blood in the urine, can be caused by diseases of the urinary system or other systemic disorders. It is classified as microscopic or gross based on visibility, and as early, terminal, or diffuse based on timing during urination. Common causes include glomerular diseases, infections, cancers, trauma, and stones. Diagnosis involves urinalysis, microscopy, imaging, and sometimes kidney biopsy. Treatment focuses on the underlying condition causing the hematuria. Prognosis depends on associated clinical or laboratory abnormalities, with isolated microscopic hematuria generally having a good prognosis.
Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by blood clots in arteries and veins, pregnancy complications, and the presence of antiphospholipid antibodies. The syndrome can occur alone or in association with other autoimmune diseases like lupus. Treatment involves long-term anticoagulation with blood thinners and aspirin to prevent new clots from forming. Management of pregnancy in APS patients depends on their history and involves low-dose aspirin with or without low or high dose blood thinners.
This document summarizes information about liver abscesses, including pyogenic and amebic types. It discusses the epidemiology, causes, clinical presentation, diagnosis, and management of both types of liver abscesses. For pyogenic liver abscesses, it notes that they are usually polymicrobial infections most commonly caused by E. coli or Klebsiella. Cryptogenic cases may indicate underlying malignancy. Diabetes is a major risk factor. Ultrasound and CT are important diagnostic tools. Treatment involves drainage and antibiotics. For amebic liver abscesses, it indicates they are endemic in India and usually caused by Entamoeba histolytica infection following travel to endemic areas. Clinical features, ultrasound and serology can aid
The document discusses various diagnostic tests and procedures. It begins by outlining the phases of diagnostic testing as pre-test, intra-test, and post-test phases. It then describes specific tests like the complete blood count, which measures components of blood, and serum electrolyte testing, which evaluates electrolyte levels important for various body functions. The document provides details on normal ranges and clinical implications of results for these common lab investigations.
Practical approach to fever with altered liver functionsikramdr01
油
This document provides information on evaluating and diagnosing a patient presenting with fever and abnormal liver function tests. It discusses the differential diagnosis, which includes conditions like malaria, typhoid, leptospirosis, viral hepatitis, infectious mononucleosis, herpes, tuberculosis, autoimmune diseases, and liver abscesses. Specific diagnostic criteria and clinical features of various conditions are outlined, along with diagnostic tests and approaches. Imaging modalities like ultrasound and their findings for conditions like cholecystitis and liver abscesses are also reviewed. The document provides an overview of evaluating causes of drug-induced liver injury.
This document discusses upper gastrointestinal bleeding (UGIB). It defines UGIB as bleeding from the gastrointestinal tract proximal to the ligament of Trietz, which usually manifests as hematemesis or melena and sometimes hematochezia. Risk stratification systems like the Blatchford and Rockall scores are used to predict outcomes like rebleeding and mortality. Endoscopy is important for diagnosis, prognosis, and potential therapy. Management involves fluid resuscitation, identifying the bleeding source, stopping active bleeding, treating underlying causes, and preventing rebleed. Proton pump inhibitors are the standard medical treatment. Endoscopic modalities like injection, thermal, and mechanical methods are used for non-variceal bleeding.
AKI, CKD, and ESRD are conditions involving the kidneys. AKI is a sudden loss of kidney function that develops over days or weeks and is often reversible. It is caused by prerenal factors like low blood pressure or intrinsic renal damage. Common causes include sepsis, low fluid intake, and medications. Diagnosis is based on increases in BUN and creatinine and decreased urine output. Treatment focuses on identifying and treating the underlying cause while managing fluid, electrolyte and acid-base imbalances. Long term kidney damage can progress to CKD or end stage renal disease requiring renal replacement therapies.
This document provides an outline for a course on childhood acute lymphoblastic leukemia (ALL). It covers the definition and epidemiology of ALL, risk factors, clinical presentation, diagnosis, management including treatment phases, complications, prognosis, and prevention. ALL is the most common childhood cancer characterized by excessive lymphoblasts. It peaks between ages 2-3 and has a survival rate over 85% with current treatments over 2-3 years consisting of induction, intensification, and maintenance chemotherapy, along with intrathecal therapy targeting the central nervous system. Complications can include tumor lysis syndrome, infections, and secondary cancers. Prognosis depends on risk factors like age and white blood cell count. Prevention focuses on limiting environmental exposures like benz
Myeloproliferative disorders include polycythemia vera, essential thrombocytosis, myelofibrosis, and chronic myeloid leukemia. Polycythemia vera is a neoplastic stem cell disorder characterized by erythrocytosis, thrombocytosis, and leukocytosis. Treatment involves phlebotomy and myelosuppressive drugs like hydroxyurea. Essential thrombocytosis is characterized by elevated platelet counts over 600,000 and enlarged, abnormal megakaryocytes. It can cause thrombosis. Myelofibrosis features bone marrow fibrosis, splenomegaly, anemia, and thrombocytopenia. Chronic myeloid leukemia is a malignant disorder caused by the Philadelphia chromosome resulting from a
BIOMECHANICS OF THE MOVEMENT OF THE SHOULDER COMPLEX.pptxdrnidhimnd
油
The shoulder complex acts as in coordinated fashion to provide the smoothest and greatest range of motion possible of the upper limb.
Combined motion of GH and ST joint of shoulder complex helps in:
Distribution of motion between other two joints.
Maintenance of glenoid fossa in optimal position.
Maintenance of good length tension
Although some amount of glenohumeral motion may occur while the other shoulder articulations remain stabilized, movement of the humerus more commonly involves some movement at all three shoulder joints.
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This patient with newly diagnosed myeloma presented with a large gluteal hematoma one week following a bone marrow biopsy. Initial workup found decreased factor XIII antigen and activity levels. Further testing showed evidence of amyloid deposits on fat pad biopsy and cardiac MRI consistent with amyloidosis, which can cause acquired bleeding disorders through effects on coagulation factors and platelets. The differential diagnosis includes evaluating for qualitative or quantitative platelet disorders, coagulation factor deficiencies, and structural causes of bleeding in the setting of a paraproteinemia like myeloma.
1) An 85-year-old woman was hospitalized for severe anemia with a hemoglobin of 3 g/dL.
2) A 76-year-old man seen for forgetfulness and difficulty walking was found to have peripheral neuropathy and anemia with hypersegmented neutrophils on blood smear.
3) A 16-year-old female with autoimmune hepatitis developed anemia with heavier menses and petechiae; bone marrow showed mild dyserythropoiesis and hypocellularity.
Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by blood clots in arteries and veins, pregnancy complications, and the presence of antiphospholipid antibodies. The condition occurs when the immune system produces antibodies that cause blood to clot abnormally. Treatment involves blood thinners and aspirin to prevent clots, with lifelong anticoagulation often needed for recurrent clotting events. Prognosis depends on symptom severity and control, with catastrophic APS having high mortality without aggressive intervention.
This document provides information about tumor lysis syndrome (TLS), including its definition, risk factors, pathophysiology, and management. TLS is an oncometabolic emergency that can occur after tumor targeted therapy leads to rapid cell death and release of cellular contents like uric acid, potassium, and phosphorus. It can cause abnormalities in electrolytes and kidney injury. High risk groups include those with hematologic malignancies like lymphoma. Management involves prevention, monitoring, volume expansion, and in some cases urinary alkalinization or allopurinol.
1. Chronic cholestasis can be caused by intrahepatic or extrahepatic conditions. Common intrahepatic causes include primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), and drug-induced liver injury (DILI).
2. PBC is an autoimmune disease characterized by progressive destruction of intrahepatic bile ducts, presence of antimitochondrial antibodies (AMA), and histologic findings of florid duct lesions on liver biopsy. PBC diagnosis requires two of three criteria: cholestatic liver enzymes, AMA positivity, or liver biopsy consistent with PBC.
3. PSC is a chronic inflammatory condition of
This document provides information on several gastrointestinal conditions:
1. Achalasia is a motility disorder of the esophagus characterized by loss of peristalsis and failure of the lower esophageal sphincter to relax properly.
2. Esophageal cancer can be squamous cell carcinoma or adenocarcinoma, with risk factors including smoking, alcohol, and Barrett's esophagus. Treatment depends on cancer stage and may include surgery, chemotherapy, or radiation.
3. Peptic ulcer disease is caused by a bacterial infection with H. pylori in most cases. Treatment involves eradicating H. pylori with antibiotic therapy and proton pump inhibitors.
The document discusses antiphospholipid syndrome (APS), a condition characterized by abnormal blood clotting caused by antibodies against phospholipids. It outlines the criteria for diagnosis, including recurrent blood clots or pregnancy loss alongside persistent antiphospholipid antibodies. Management involves long-term anticoagulation for clots and aspirin with heparin during pregnancy to prevent complications. A rare but severe form called catastrophic APS can affect multiple organs and requires aggressive treatment.
Hematuria, or blood in the urine, can be caused by diseases of the urinary system or other systemic disorders. It is classified as microscopic or gross based on visibility, and as early, terminal, or diffuse based on timing during urination. Common causes include glomerular diseases, infections, cancers, trauma, and stones. Diagnosis involves urinalysis, microscopy, imaging, and sometimes kidney biopsy. Treatment focuses on the underlying condition causing the hematuria. Prognosis depends on associated clinical or laboratory abnormalities, with isolated microscopic hematuria generally having a good prognosis.
Antiphospholipid syndrome (APS) is an autoimmune disorder characterized by blood clots in arteries and veins, pregnancy complications, and the presence of antiphospholipid antibodies. The syndrome can occur alone or in association with other autoimmune diseases like lupus. Treatment involves long-term anticoagulation with blood thinners and aspirin to prevent new clots from forming. Management of pregnancy in APS patients depends on their history and involves low-dose aspirin with or without low or high dose blood thinners.
This document summarizes information about liver abscesses, including pyogenic and amebic types. It discusses the epidemiology, causes, clinical presentation, diagnosis, and management of both types of liver abscesses. For pyogenic liver abscesses, it notes that they are usually polymicrobial infections most commonly caused by E. coli or Klebsiella. Cryptogenic cases may indicate underlying malignancy. Diabetes is a major risk factor. Ultrasound and CT are important diagnostic tools. Treatment involves drainage and antibiotics. For amebic liver abscesses, it indicates they are endemic in India and usually caused by Entamoeba histolytica infection following travel to endemic areas. Clinical features, ultrasound and serology can aid
The document discusses various diagnostic tests and procedures. It begins by outlining the phases of diagnostic testing as pre-test, intra-test, and post-test phases. It then describes specific tests like the complete blood count, which measures components of blood, and serum electrolyte testing, which evaluates electrolyte levels important for various body functions. The document provides details on normal ranges and clinical implications of results for these common lab investigations.
Practical approach to fever with altered liver functionsikramdr01
油
This document provides information on evaluating and diagnosing a patient presenting with fever and abnormal liver function tests. It discusses the differential diagnosis, which includes conditions like malaria, typhoid, leptospirosis, viral hepatitis, infectious mononucleosis, herpes, tuberculosis, autoimmune diseases, and liver abscesses. Specific diagnostic criteria and clinical features of various conditions are outlined, along with diagnostic tests and approaches. Imaging modalities like ultrasound and their findings for conditions like cholecystitis and liver abscesses are also reviewed. The document provides an overview of evaluating causes of drug-induced liver injury.
This document discusses upper gastrointestinal bleeding (UGIB). It defines UGIB as bleeding from the gastrointestinal tract proximal to the ligament of Trietz, which usually manifests as hematemesis or melena and sometimes hematochezia. Risk stratification systems like the Blatchford and Rockall scores are used to predict outcomes like rebleeding and mortality. Endoscopy is important for diagnosis, prognosis, and potential therapy. Management involves fluid resuscitation, identifying the bleeding source, stopping active bleeding, treating underlying causes, and preventing rebleed. Proton pump inhibitors are the standard medical treatment. Endoscopic modalities like injection, thermal, and mechanical methods are used for non-variceal bleeding.
AKI, CKD, and ESRD are conditions involving the kidneys. AKI is a sudden loss of kidney function that develops over days or weeks and is often reversible. It is caused by prerenal factors like low blood pressure or intrinsic renal damage. Common causes include sepsis, low fluid intake, and medications. Diagnosis is based on increases in BUN and creatinine and decreased urine output. Treatment focuses on identifying and treating the underlying cause while managing fluid, electrolyte and acid-base imbalances. Long term kidney damage can progress to CKD or end stage renal disease requiring renal replacement therapies.
This document provides an outline for a course on childhood acute lymphoblastic leukemia (ALL). It covers the definition and epidemiology of ALL, risk factors, clinical presentation, diagnosis, management including treatment phases, complications, prognosis, and prevention. ALL is the most common childhood cancer characterized by excessive lymphoblasts. It peaks between ages 2-3 and has a survival rate over 85% with current treatments over 2-3 years consisting of induction, intensification, and maintenance chemotherapy, along with intrathecal therapy targeting the central nervous system. Complications can include tumor lysis syndrome, infections, and secondary cancers. Prognosis depends on risk factors like age and white blood cell count. Prevention focuses on limiting environmental exposures like benz
Myeloproliferative disorders include polycythemia vera, essential thrombocytosis, myelofibrosis, and chronic myeloid leukemia. Polycythemia vera is a neoplastic stem cell disorder characterized by erythrocytosis, thrombocytosis, and leukocytosis. Treatment involves phlebotomy and myelosuppressive drugs like hydroxyurea. Essential thrombocytosis is characterized by elevated platelet counts over 600,000 and enlarged, abnormal megakaryocytes. It can cause thrombosis. Myelofibrosis features bone marrow fibrosis, splenomegaly, anemia, and thrombocytopenia. Chronic myeloid leukemia is a malignant disorder caused by the Philadelphia chromosome resulting from a
BIOMECHANICS OF THE MOVEMENT OF THE SHOULDER COMPLEX.pptxdrnidhimnd
油
The shoulder complex acts as in coordinated fashion to provide the smoothest and greatest range of motion possible of the upper limb.
Combined motion of GH and ST joint of shoulder complex helps in:
Distribution of motion between other two joints.
Maintenance of glenoid fossa in optimal position.
Maintenance of good length tension
Although some amount of glenohumeral motion may occur while the other shoulder articulations remain stabilized, movement of the humerus more commonly involves some movement at all three shoulder joints.
The course covers the steps undertaken from tissue collection, reception, fixation,
sectioning, tissue processing and staining. It covers all the general and special
techniques in histo/cytology laboratory. This course will provide the student with the
basic knowledge of the theory and practical aspect in the diagnosis of tumour cells
and non-malignant conditions in body tissues and for cytology focusing on
gynaecological and non-gynaecological samples.
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・ Watch Now: https://www.nuaire.com/resources/best-sampling-practices-cleanroom-usp-797
Stay informedfollow Abby Roth on LinkedIn for more cleanroom insights!
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14. Definitions
PANCYTOPENIA:-
Decreases in all peripheral blood lineages
BiCYTOPENIA:-
Decreases in two peripheral blood lineages
LEUKOPENIA:-
Decrease in WBCs count (<4400 cells/microL in most
clinical laboratories)
15. How to approach
HISTORY EXAMINATION LAB TEST
Hematology
Referral
INITIAL FURTHER
CBC
CMP
Peripheral
smear
Retics Count
Coagulation
profile
Blood grouping
Case based e.g
Bone
marrow
Imaging
Endosco
pies
Less Urgent No referral
Emergency
16. Neutropenia
Mild ANC 1000 and <1500 cells/microL
Moderate ANC 500 and <1000 cells/microL
Severe ANC <500 cells/microL
Agranulocytosis ANC <200 cells/microL
Chronic neutropenia Neutropenia for >3 months
Constitutional neutropenia Longstanding neutropenia, typically since
childhood
Granulocytopenia Reduced number of neutrophils, eosinophils, and
basophils
Isolated neutropenia Neutropenia without associated anemia and/or
thrombocytopenia
17. Absolute neutrophil count The absolute neutrophil count (ANC) is the number of
neutrophils plus bands, but does not include metamyelocytes and less mature forms.
ANC = WBC (cells/microL) x percent (PMNs + bands) 歎 100
18. Mechanisms of PANCYTOPENIA
1. Bone marrow infiltration/replacement
2. Bone marrow aplasia
3. Blood cell destruction or sequestration
20. When to repeat CBC?
If mild and patient is well
Repeat in 1-2 weeks, and if persistently low after 6 weeks, then
needs further investigation and to refer him to hematology
If moderate or severe
If unwell of febrile, urgent referral
If patient is well, repeat CBC after 2 weeks (safety netting)
QUESTION
ANSWER
21. HISTORY
Time course and clinical severity
Symptoms associated with pancytopenia
Recurrent, severe, or unusual infections Fatigue, dyspnea, chest pain,
hemodynamic instability, or claudication due to anemia
Bleeding or easy bruising
Fever, night sweats, and/or weight loss
Nausea, vomiting, and jaundice that may be associated with liver disease
Previous treatments
Other medical conditions
Problematic medications
Personal and occupational exposures
22. Rashes that may be related to drug reactions, rheumatologic disorders,
infections, and malignancies
Oral lesions; as examples, thrush suggests immune compromise; oral
ulcers may be seen in diseases such as systemic lupus erythematosus
Lymphadenopathy and/or splenomegaly
Jaundice and stigmata of liver disease
EXAMINATION
24. Not usually clinically significant
Lymphocytopenia
Normal range 1.0-4.0 X 109
/L
It represents 20-40%
26. 19-year-old male, not known to have any chronic illnesess
presented to the clinic with generalized weakness, backache,
and significant weight loss for the past 2 years. He was taking
B12 and folic acid plus Iron as supplementations for 2 months
prior to presentation.
On examination
Mild pallor, massive splenomegaly to the level of the umbilicus,
and mild hepatomegaly
28. Leukocytosis refers to elevated WBC (leukocyte) count. Neutrophilia is the
most common type of leukocytosis, but leukocytosis may also be due to
increased monocytes, eosinophils, basophils, and/or lymphocytes
Granulocytosis is often used interchangeably with neutrophilia, but
granulocytosis is a broader term that can also reflect increased eosinophils or
basophils.
Left shift is an ill-defined term that refers to an increase in the percentage of
band forms, generally accompanied by metamyelocytes and myelocytes.
Leukemoid reaction refers to WBC >50,000/microL from causes other than
leukemia, with the majority being mature neutrophils, often accompanied by
increased numbers of bands, metamyelocytes, and/or myelocytes
LEUKOCYTOSIS
29. Approach to the patient with neutrophilia
HISTORY EXAMINATION LAB TEST Special Testing
CBC
Peripheral Smear
Active or prior infection or inflammation
Hematologic malignancies
Surgical or functional asplenia
Cigarette smoking
Vigorous exercise
Extreme physical or emotional distress
Conditions that may be associated with neutrophilia (eg,
pregnancy, eclampsia, post-partum, thyroid storm,
hypercortisolism)
Family history
Bone marrow aspirate and biopsy
Flow cytometry
Molecular/genetic testing
30. How to differentiate between Leukemoid reaction and CML ?
The LAPscore is raised in Leukemoid reaction whereas
decreased in CML
Presence of left shift in CML
Prominence of Myelocytes in CML
May be Eosinphilia and/or Basophilia in CML
QUESTION
ANSWER
31. MECHANISMS
Increased production of neutrophils
Autonomous (ie, due to malignant disorders such as
myeloproliferative neoplasms)
Reactive (ie, in response to infectious or inflammatory
processes)
33. How to follow a patient with an isolated neutrophilia ?
If patient is well
1-2 months, then 3 monthly for 12 months.
Stop monitoring if normal
QUESTION
ANSWER