Thymoma

Thymoma

Exam2

Exam2

Cushing syndrome
Pheochromocytoma
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Adrenal cortical carcinoma
Conn syndrome
Thyroglossal duct cyst
Hyperthyroidism
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Thyroid storm
Hypothyroidism
Euthyroid sick syndrome
Hashimoto thyroiditis
Subacute granulomatous thyroiditis
Riedel thyroiditis
Thyroid cancer
Hyperparathyroidism
Hypoparathyroidism
Hypercalcemia
Hypocalcemia
Diabetes mellitus
Diabetic retinopathy
Diabetic nephropathy
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Pituitary apoplexy
Sheehan syndrome
Hypoprolactinemia
Constitutional growth delay
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Multiple endocrine neoplasia
Pancreatic neuroendocrine neoplasms
Zollinger-Ellison syndrome
Carcinoid syndrome
Neuroblastoma
Opsoclonus myoclonus syndrome (NORD)
Adrenal insufficiency: Pathology review
Adrenal masses: Pathology review
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Thyroid nodules and thyroid cancer: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Diabetes mellitus: Pathology review
Cushing syndrome and Cushing disease: Pathology review
Pituitary tumors: Pathology review
Hypopituitarism: Pathology review
Diabetes insipidus and SIADH: Pathology review
Multiple endocrine neoplasia: Pathology review
Iron deficiency anemia
Beta-thalassemia
Alpha-thalassemia
Sideroblastic anemia
Anemia of chronic disease
Lead poisoning
Hemolytic disease of the newborn
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Paroxysmal nocturnal hemoglobinuria
Sickle cell disease (NORD)
Hereditary spherocytosis
Aplastic anemia
Fanconi anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Diamond-Blackfan anemia
Acute intermittent porphyria
Porphyria cutanea tarda
Hemophilia
Vitamin K deficiency
Bernard-Soulier syndrome
Glanzmann's thrombasthenia
Hemolytic-uremic syndrome
Thrombotic thrombocytopenic purpura
Von Willebrand disease
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Antiphospholipid syndrome
Hodgkin lymphoma
Non-Hodgkin lymphoma
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Type I hypersensitivity
Food allergy
Anaphylaxis
Asthma
Type II hypersensitivity
Rheumatic heart disease
Myasthenia gravis
Pemphigus vulgaris
Type III hypersensitivity
Serum sickness
Systemic lupus erythematosus
Poststreptococcal glomerulonephritis
Type IV hypersensitivity
Graft-versus-host disease
Contact dermatitis
X-linked agammaglobulinemia
Selective immunoglobulin A deficiency
Common variable immunodeficiency
IgG subclass deficiency
Hyperimmunoglobulin E syndrome
Isolated primary immunoglobulin M deficiency
Thymic aplasia
DiGeorge syndrome
Severe combined immunodeficiency
Adenosine deaminase deficiency
Ataxia-telangiectasia
Hyper IgM syndrome
Wiskott-Aldrich syndrome
Leukocyte adhesion deficiency
Chediak-Higashi syndrome
Chronic granulomatous disease
Complement deficiency
Hereditary angioedema
Asplenia
Thymoma
Ruptured spleen
Immunodeficiencies: T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Combined T-cell and B-cell disorders: Pathology review
Immunodeficiencies: Phagocyte and complement dysfunction: Pathology review

Flashcards

Thymoma

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Questions

USMLE® Step 1 style questions USMLE

0 of 3 complete

Start
A 40-year-old woman begins complaining of dyspnea while recovering in the post-anesthesia care unit. Earlier in the day, the patient underwent a laparoscopic cholecystectomy for treatment of symptomatic gallstones. Past medical history is unremarkable. Her temperature is 37.7°C (99.9°F), pulse is 93/min, respiratory rate is 24/min and blood pressure is 125/72 mmHg. Physical examination shows the patient in distress with shallow breaths, using accessory muscles. In addition, the patient is observed to have drooping of the eyelids and corners of the mouth bilaterally. Pupils are 3 cm bilaterally and reactive to light. An arterial blood gas measurement reveals the following findings:  

 Laboratory Value  Result  Reference Range 
 pH  7.31  7.35-7.45 
 PaCO2  56 mmHg  33-45 mmHg 
 PaO2  71 mmHg  75-105 mmHg 
 Bicarbonate  25 mmol/L  22-28 mmol/L 
   
The patient’s condition improves with administration of edrophonium chloride. Which of the following best describes the cause of this patient’s condition? 

Key Takeaways

Thymoma is a rare type of tumor that arises from the epithelial cells of the thymus gland that is located in the chest behind the breastbone. Thymomas may not cause any symptoms in the early stages of the disease, but as they grow and compress the nearby structures, causing symptoms like superior vena cava syndrome, dysphagia, cough, or chest pain.

Thymomas are frequently associated with the neuromuscular disorder myasthenia gravis or autoimmune conditions like pure red cell aplasia and Good syndrome. Diagnosis of thymoma involves imaging studies such as CT or MRI scans. A biopsy may also be performed to confirm the diagnosis. Treatment options may include surgery to remove the tumor, radiation therapy, chemotherapy, or a combination of these approaches.