Step 2CK/Step 3 Flashcards
In which demographic do cavernous hemangiomas present?
What is a possible complication of a visceral hemangioma?
Kids; cavernous=strawberry hemangioma (can be bluish if it is deeper; less likely to regress)
Visceral hemangioma: High output heart failure
How do you differentiate osteoid osteoma from osteoblastoma?
Osteoid osteoma (OO) is in long bones and pain responds to aspirin
Osteoblastoma (OB) is larger than 2cm, happens in vertebrae and it’s pain doesn’t decrease with aspirin
Presentation, macro and histological hallmarks of Osteoid Osteoma:
OhOh: little benign thing on the cortex that goes away with aspirin
Presentation: Benign, in younger than 25, less than 2cm and pain at night relieved by NSAIDs
Macro: on the cortex of the diaphysis (side), Rx radiolucent core of osteoid (dark) surrounded by sclerosis (white)
Micro: woven bone lined by a single layer of ~blasts
Presentation, macro and histological hallmarks of OsteoChondroma:
OC tv show: young, mushroom
Presentation: most frequent benign, in younger than 25, mushroom shape, condro part can transform in chondrosarcoma
Macro: bony spike covered by a cartilage cap on the metaphysis (almost tip)
Micro: spike is continuous wit the marrow
Presentation, macro and histological hallmarks of ChondroSarcoma:
CaSa: elder, pelvis
Presentation: in adults older than 50 around the pelvis!
Macro: moth eaten lytic appearance with popcorn-like spiculated calcifications in Rx
Micro: irregular cartilage and calcifications
Presentation, macro and histological hallmarks of giant cell/osteoclatoma:
Presentation: benig but locally aggressive and may recur. Female=male
Macro: on the epiphysis!!! (tip) of the knee. Rx soap bubble. Nonsclerotic sharply defined border
Micro: tumor cells with RANK-L (~blasts) and multinucleated giant cells (~clasts)
Presentation, macro and histological hallmarks of OsteoSarcoma/ osteogenic sarcoma:
OSsss: the most frequent malignant ‘sssss’
Presentation: Most common malignant. Painful enlarging mass or fracture. Bimodal distribution in teenagers (retinoblastoma) and elderly (Paget’s, radiation). Aggressive
Macro: on the metaphysis (almost tip) of the knee. Rx Codman triangle (periostial elevation, swelling) or sunburst (lytic, tiny fragments of bone)
Micro: plemomorphic cells making osteoid; malignant proliferation of osteoblasts (spindle shaped pink)
Malignant osteoblasts arise form mesenchymal stem cells in the PERIOSTEUM
Presentation, macro and histological hallmarks of Ewing sarcoma:
Presentation: 2nd most common malignant. Painful and swelling, ±fever, boys, good px
Macro: on the diaphysis of femur, grows inside the narrow and pressures the periosteum that grows on onion skin reaction and moth eaten appearance (means extension to the soft tissue)
Micro: mesenchymal but small blue w Homer-Wright pseudorosettes and glycogen +CD99, +MIC2, t(11;22) EWS-FLI1 for DD with lymphoma and osteomyelitis
Tto: sx or Dactinomycin (drug for kid tumors)
Clinic and how you differentiate α-thalassemia minor and β-thalassemia minor?
Both are normal but become anemic when they are under stress, have target cells
α has normal electrophoresis
β has aBnormal electrophoresis ↑HbA2(2α2δ) ↑HbF(2α2γ)
What is the treatment for magnesium overdose?
IV calcium gluconate
What do nodules with spiculated borders in chest Rx indicate? What is the management?
Lung ca, due to malignant cells extending within pulmonary interstitial tissue (stippled, irregular or eccentric calcifications also indicate malignancy but popcorn or bull’s eye calcifications indicate benign nodule).
1) Ask for previous Rx, if lesion has been stable 2-3 years you are done
2) Chest CT:
- Benign: less than 40 y.o, less than 0.8cm, never smoker or more than 15y since stopped, smooth → serial CTs
- Intermediate: 40-60//0.8-2//smoker or 15-5, scalloped → biopsy* or PET
*Biopsy:
Central: bronchoscopy
Peripheral: CT-guided - High risk: more than 60y.o, more than 2cm, smoker or less than 5y since stopped, corona radiata or spiculated → sx
Malignant pleural effusion makes lung ca. inoperable
Which parameter increase when you lower the GUIDELINE’S cutoff for diagnosis? What about when you lower the cutoff of a NEW TEST to diagnose the disease?
What happens if you do the same test on a healthier (younger) population?
Lower GUIDELINE’S cutoff for diagnosis: ↑ prevalence. ‘A medical association changes the guidelines so more people are actually sick’
↑ sensitivity and NPV. ‘A new test positive cutoff changes but the gold standard and therefore the actual number of sick people remains the same’
↓ prevalence, ↓ PPV, ↑ NPV, =sensitivity and =specificity
What do you think about if you see a middle easter male with abdominal mass in the gut, mesenteric lymph nodes and malabsorption?
IgA heavy chain disease= mediterranean lymphoma= Seligmann disease
Biopsy: jejunal mucosal infiltration with plasmacytoid cells
What is important to do after diagnosing Raynauds?
Nailfold microscopy to look for enlarged distorted or scarce capillaries because if you see those, they indicate secondary Raynauds normally due to mixed connective tissue diseases as scleroderma
Fetty syndrome signs and symptoms:
RA+ neutropenia+ splenomegally (anemia and thrombocytopenia are possible)
What is the management of head and neck squamous cell ca?
And of a parotid tumor?
Squamous cell ca:
1) Ultrasound and fine needle aspiration
2) Panendoscopy (endoscopy of larynx, bronchus and esophagus) to find the ca.
Endoscope-guided biopsy for nasopharyngeal ca. → RT+QT
Parotid:
1) Fine needle aspiration
2) If non-dx fine needle aspiration of an enlarging parotid mass
3) Superficial parotidectomy (that is also curative for most benign parotid tumors)/deep parotidectomy*
If metastasis do a modified radical neck dissection + postsx RT
What should you think about if you see a kid with RBC aplasia?
Transient erythroblastopenia of childhood, it is transient and normally due to a virus
Decreased reticulocytes
Normal MCV!!
Recovers in 1-2mo
NBSM; no need marrow aspirate; you just need to FOLLOW Hb for 2-3mo until resolution!!!
Which malignancy can lead to sideroblastic anemia?
Myelodisplastic syndrome
What is a different name for Wilms tumor?
Nephroblastoma
What are the main symptoms and the possible treatments for essential thrombocythemia?
Vasomotor symptoms: headaches…
Treatments: Low-dose aspirine Hydroxyurea (avoid in pregnancy) Anagrelide Plateletpheresis
QT regimes for ALL, CLL, Hodgkin and Non-Hodgkin lymphoma:
ALL:
Daunorubicin, Vincristine and Prednisone
AML:
Daunorubicin and cytosine arabinoside (AraC)
CLL:
Fludrabine and Chlorambucil (do not treat if asymptomatic and stage less than 3)
Hodgkin:
ABVD
Adriamycin (doxorubicin), Bleomycin, Vinblastine, Dacarbazine
Non-Hodgkin:
R-CHOP
Rituximab, Cyclophosphamide, Hydroxydaunorubicin, Oncovin (Vincristine) and Prednisolone
How do you prevent tumor lysis sd? How do you treat it? Which drug is contraindicated? Which are some of the SE of these drugs?
Prevention:
Allopurinol and febuxostat (febuxostat is better for the kidney than allopurinol); inhibit xanthine oxidase
* they do not decrease the amount uric acid that already exists (SE: Steven-Johnson and renal stones)
Treatment:
Rasburicase and pegloticase; recombinant urate oxidase that convert uric acid in allantoin (SE: G6PD hemolysis, anaphylaxis!, methemoglobinemia)
Add Ca supplementation to prevent hypocalcemia
Contraindicated:
Probenecib!!! uricosuric agent that blocks the reabsorption of uric acid at the PCT
Urinary sample markers of pheochromocytoma and neuroblastoma vs carcinoid tumor:
Pheochromocytoma and Neuroblastoma: make epi, NE and DA so in urine you see homovanillic and vanillylmandelic acid. Also, if you don’t find the mass on CT scan you can check for ↑ uptake of iodine-131-metaiodobenzylguanidine = I-131 MIBG!!
Carcinoid: makes 5HT so in urine you see 5-hydroxyindoleacetic acid → CT scan → Octreotide scintigraphy if CT does not find the tumor
Before electrophoresis, how can you differentiate between iron deficiency anemia and thalassemia?
Iron deficiency anemia:
↑ red cell distribution width (RDW)
MCV/RBC count (Mentzer ratio) more than 13
↓ reticulocytes
Suspect it on a kid having mostly cow’s milk before 1y, also all breast fed babies should be started on 400IU within 1mo
Thalassemia:
Nr RDW
Mentzer ratio less than 13
↑ reticulocytes