DIVINE! Flashcards
Sickle cell disease vaccines?
SHIN
Streptococcus Pneumonia
Haemophilus influenzae
Neisseria Meningitidis
(also klebsiella and and psuedomonas)
Light’s Criteria!
- Pleural fluid protein/serum protein < 0.5
- Pleural fluid LDH/serum LDH < 0.6
- Pleaural fluid LDH < 0.67 ULN of serum LDH.
- If one of these rules are violated, the fluid is exudative (malignancy, PE, ARDS)
- Normal pleural fluid pH is 7.6
- Transudative fluid is 7.4-7.55
- Exudative is 7.3-7.45
Common causes of pleural effusions?
- Transudative
- CHF
- Cirrhosis
- Nephrotic Syndrome
- Peritoneal dialysis
- Exudative
- infections
- malignancy
- Inflammatory disorders
- Fluid from abdomen to pleural space
- coronary artery bypass surgery
- pulmonary embolism
RUQ pain, fever, +ve Murphy’s sign
Cholecystitis
RUQ pain, fever, scleral icterus, BP 80/48 (hypotension), altered MS
Ascending cholangitis
HLA-B27 diseases?
PAIR
Psoriasis
Ankylosing Spondylitis
Irritable bowel disease
Reiter’s Syndrome (reactive arthritis post bacterial infection, re-can’t see; uveitis, can’t pee; urethritis, can’t climb a tree; arthritis)
MEN syndomes?
- MEN1 (3 Ps)
- Pituitary adenoma
- Parathyroid hyperplasia
- Pancreatic islet cell tumors (gastrinoma, insulinoma, glucagonoma)
- MEN2a (MPH)
- Calcitonin (medullary carcinoma of the thyroid with elevated calcitonin level)
- Calcium (parathyroid hyperplasia, which causes elevated calcium levels)
- Catecholamines which are made in the chromocytes (as in pheochromocytoma)
- MNE2b (MPM)
- Medullary thyroid carcinoma
- Pheochromocytoma
- Mucosal neuromas
MEN1
- Hypercalcemia: brittle bones (fractures, due to osteoporosis), kidney stones, abdominal moans (abdominal pain), and psychiatric overtones (confusion).
- Treatment-resistant peptic ulcer disease (gastrinoma) or hypoglycemia (insulinoma).
MEN2A
- Hypercalcemia: brittle bones (fractures, due to osteoporosis), kidney stones, abdominal moans (abdominal pain), and psychiatric overtones (confusion).
- Severe, treatment-resistent hypertension (particularly paroxysmal in nature, with headaches, palpitations, and diaphoresis).
Child with retinoblastoma, cancer later?
Osteosarcoma
CLL
indolent, derived from B cells, CD5+ (usually only in T cells). smude cells on histology, SEVERE leukocytosis
Multiple myeloma
CRAB symptoms
hyperCalcemia
Renal insufficiency
Anemia
Bone pain
65 yo M with pancytopenia. A peripheral smear reveals tear drop shaped RBCs
Primary myelofibrosis
88 yo F has a 6 mo hx of recurrent infections. WBC is 87000. A peripheral smear reveals “smudge cells”
CLL
78 yo M. A peripheral smear is notable for RBCs stacked like coins
Multiple myeloma (Rouleaux formatin)
78 yo M with pancytopenia. Bone marrow aspiration is consistent with a “dry tap”-
Primary myelofibrosis
66 yo F presents with a 6 mo hx of recurrent infections, WBC is 47k with a preponderance of cells in different stages of maturation. These cells have reduced leukocyte alkaline phosphatase activity-
CML (9/22 translocation, Philadelphbia, give imatinib)
55 yo M is S/P Day 5 from recent treatment for a hematologic malignancy. Plts are 40K, D-dimers are elevated, he is bleeding from every IV Site-
Acute promyelocytic leukemia (Auer rods can trigger DIC, low plts, High FDPs/PT/PTT, give ATRA to promote myeloblast maturation)
5 yo F presents with a 6 week hx of weight loss and fever. CBC is notable for pancytopenia. Cytologic studies reveal TDT +ve cells
ALL
55 yo M presents with fever, weight loss, and night sweats. Peripheral smear reveals B cells with a bilobate nucleus
Hodgkin’s lymphoma
45 yo F with a hx of CML presents with a 3 week hx of diffuse lymphadenopathy and fever-
AML
45 yo F with a 6 month history of intense pruritus. BMP is notable for conjugated hyperbilirubinemia. Abdominal imaging reveals dilation of intrahepatic bile ducts
This is primary biliary cholangitis associated with anti-mitochondrial antibodies. Treatment involves the use of Ursodiol. Liver transplantation is the only definitive treatment.
45 yo M with a history of ulcerative colitis presents with a 6 month history of pruritus. Abdominal imaging reveals dilation of intra and extrahepatic bile ducts
this is Primary Sclerosing Cholangitis associated with p-ANCA. Note the difference in biliary duct pathology. Ursodiol does not work as well here. Liver transplantation and occasionally endoscopic dilation of strictures may suffice.
25 yo M presents with a multi year history of sinusitis, hemoptysis, and hematuria
Wegener’s granulomatosis. Associated with c-ANCA. Could present as RPGN. Treat with steroids and cyclophosphamide.
25 yo M presents with new onset asthma. Urinalysis reveals dysmorphic erythrocytes
this is Churg-Strauss Syndrome. Associated with p-ANCA (like microscopic polyangiitis). Consider this diagnosis in the setting of asthma and associated RPGN/nephritic syndromes.
35 yo F presents with episodic discoloration of her fingers when she steps out of her home in winter. PE is notable for diffuse skin thickening
scleroderma (anticentromere antibodies for CREST scleroderma), anti-SCL 70 (topoisomerase) for diffuse scleroderma.