Beruflich Dokumente
Kultur Dokumente
subtitle style
Medical History
Medical History
General Data
A.D.L. 60 years old Female Filipino Married Catholic Pasay City Admitted in our institution last June 08, 2011
Chief Complaint
(-) difficulty in breathing (-) dysphagia (-) palpitations (-) weight loss (-) change in bowel habits (-) tremors (-) medications taken
(+) Hypertension Norvasc, Simvastatin (-) Diabetes mellitus (-) Asthma (-) Lung Disease/Tuberculosis (-) Allergies (+) Appendectomy 1965 (+) Excision of sinus polyp - 2006
(+) Hypertension mother (+) Asthma - mother (-) Diabetes Mellitus (-) Cancer (-) Lung Disease
(-) Cigarette Smoking (-) Alcoholic Beverage Drinking (-) Allergies to food and drug
Review of Systems
General. (-) weakness, fatigue, fever Skin. (-) rashes, sores, pruritus HEENT. (-) headache, head injury, dizziness, abnormal vision, eye pain, redness, blurred vision, spots, specks, tinnitus, earaches, ear discharge, epistaxis, sore throat, hoarseness Neck. (-) stiff neck Breasts. (-) lumps, discharge, palpable mass
Review of Systems
Respiratory. (-) cough, hemoptysis CVS. (-) chest pain, othopnea, paroxysmal nocturnal dyspnea, edema GIT. (-) loss of appetite, nausea, change in bowel habits, rectal bleeding, hemorrhoids, abdominal pain, jaundice GUT. (-) dysuria, nocturia, hematuria, frequency, incontinence Neurologic. (-) fainting, seizures, weakness, tremors, numbness
Review of Systems
Hematologic. (-) easy bruising, past transfusion Endocrine. (-) excessive thirst, polyuria Psychiatric. (-) memory changes
Physical Examination
Vital Signs
HEENT
Anicteric sclera Pink Palpebral conjunctiva (-) nasal discharge (-) ear discharge (-) CLAD 2x3 cm anterior neck mass, right, firm, non tender, moves with deglutition 1x1 cm anterior neck mass, left, firm non tender, moves with deglutition
Symmetric Chest Expansion (-) intercostal retractions Clear Breath Sounds (-) rales / wheezing
Cardiovascular System
Abdomen
Extremities
Full and Equal Peripheral Pulses Pink nail beds (-) edema (-) cyanosis
Pertinent Findings
Subjective
60 year old, female Anterior neck mass (-) palpitations (-) tremors (-) weight changes (-) heat or cold intolerance (-) changes in bowel habits
Pertinent Findings
Objective
(-) CLAD 2x3 cm anterior neck mass, right, firm, non tender, moves with deglutition 1x1 cm anterior neck mass, left, firm non tender, moves with deglutition
Admitting Diagnosis
Differential Diagnosis
Hashimoto Thyroiditis
Ruled in
Ruled out
Differential Diagnosis
Riedel Thyroiditis
Ruled in
Common in women Painless anterior neck mass Hard woody neck mass Fixed Produce symptoms of compression including dysphagia, dyspnea, choking, and hoarseness
Ruled out
Patient was admitted at the ward. Patient underwent total thyroidectomy. Patient tolerated the procedure well.
Final Diagnosis
CASE DISCUSSION
Goiter
Any enlargement of the thyroid gland is referred to as a goiter Enlarges in order to maintain the patient in a euthyroid state May be diffuse, uninodular, or multinodular
Presentation
asymptomatic, although patients often complain of a pressure sensation in the neck, particularly with motion. As the goiters become very large, compressive symptoms, such as dyspnea and dysphagia Pemberton's signfacial flushing and dilatation of cervical veins upon raising the arms above the head substernal goiter
Presentation
Physical examination may reveal a soft, diffusely enlarged gland (simple goiter) or nodules of various size and consistency in case of a multinodular goiter. Deviation of the trachea may be apparent.
Treatment
Most euthyroid patients with small, diffuse goiters do not require treatment Endemic goiters are treated by iodine administration
Treatment
continue to increase despite T4 suppression, cause obstructive symptoms, have substernal extension, are suspected to be malignant or are proven malignant by FNA biopsy, cosmetically unacceptable
RET proto-oncogene plays a significant role in the pathogenesis of thyroid cancers. It is located on chromosome 10 and encodes a receptor tyrosine kinase
Papillary Carcinoma
80% of all thyroid malignancies in iodine-sufficient areas and is the predominant thyroid cancer in children and individuals exposed to external radiation occurs more often in women, with a 2:1 female:male ratio the mean age at presentation is 30 to 40 years
Papillary Carcinoma
Lymph node metastases are common, especially in children and young adults, and may be the presenting complaint Diagnosis is established by FNA biopsy of the thyroid mass or lymph node
Papillary Carcinoma
Macroscopic calcification, necrosis, or cystic change may be apparent generally hard and whitish and remain flat on sectioning with a blade Histologically, papillary carcinomas may exhibit papillary projections, a mixed pattern of papillary and follicular structures, or a pure follicular pattern (follicular variant)
Papillary Carcinoma
Cells are cuboidal with pale, abundant cytoplasm, "grooving," crowded nuclei, and intranuclear cytoplasmic inclusions, Orphan Annie nuclei excellent prognosis with a greater than 95% 10-year survival rate Most authors agree that patients with high-risk tumors or bilateral tumors should undergo total or near-total thyroidectomy
Follicular Carcinoma
10% of thyroid cancers and occur more commonly in iodine-deficient areas Women have a higher incidence of follicular cancer, with a female:male ratio of 3:1, mean age at presentation of 50 years. present as solitary thyroid nodules, occasionally with a history of rapid size increase, and long-standing goiter. Pain is uncommon, unless hemorrhage into the nodule has occurred
Follicular Carcinoma
Histologically, follicles are present, but the lumen may be devoid of colloid. Malignancy is defined by the presence of capsular and vascular invasion Patients diagnosed by FNA biopsy as having a follicular lesion should undergo thyroid lobectomy
Follicular Carcinoma
Intraoperative frozen-section examination usually is not helpful, but should be performed when there is evidence of capsular or vascular invasion, or when adjacent lymphadenopathy is present. Total thyroidectomy should be performed when thyroid cancer is diagnosed.
Like follicular cancers, Hrthle cell cancers are characterized by vascular or capsular invasion, and therefore cannot be diagnosed by FNA biopsy. more often multifocal and bilateral (approximately 30%), usually do not take up RAI (approximately 5%), more likely to metastasize to local nodes (25%) and distant sites, associated with a higher mortality rate
Medullary Carcinoma
5% of thyroid malignancies and arise from the parafollicular or C cells of the thyroid C cells secrete calcitonin, a 32-amino-acid polypeptide that functions to lower serum calcium levels typically unilateral (80%) in patients with sporadic disease, and multicentric in familial cases, with bilateral tumors occurring in up to 90% of familial patients
Medullary Carcinoma
Microscopically, tumors are composed of sheets of infiltrating neoplastic cells separated by collagen and amyloid Diagnosis is established by history, physical examination, raised serum calcitonin or CEA levels, and FNA cytology of the thyroid mass Total thyroidectomy
Anaplastic Carcinoma
approximately 1% of all thyroid malignancies majority of tumors present in the seventh and eighth decades of life typical patient has a long-standing neck mass, which rapidly enlarges and may be painful Lymph nodes usually are palpable at presentation Confirmed by FNA biopsy revealing characteristic giant and multinucleated cells.
Anaplastic Carcinoma
gross inspection, anaplastic tumors are firm and whitish in appearance Microscopically, sheets of cells with marked heterogeneity are seen. Cells may be spindle-shaped, polygonal, or large, multinucleated cells.
Anaplastic Carcinoma
gross inspection, anaplastic tumors are firm and whitish in appearance Microscopically, sheets of cells with marked heterogeneity are seen. Cells may be spindle-shaped, polygonal, or large, multinucleated cells. Tumor is one of the most aggressive thyroid malignancies, with few patients surviving 6 months beyond diagnosis
Lymphoma
less than 1% of thyroid malignancies and most are of the non-Hodgkin's B-cell type most thyroid lymphomas develop in patients with chronic lymphocytic thyroiditis rapidly enlarging neck mass often is painless diagnosis usually is suggested by FNA biopsy, although needle-core or open biopsy may be necessary for definitive diagnosis
Lymphoma
less than 1% of thyroid malignancies and most are of the non-Hodgkin's B-cell type most thyroid lymphomas develop in patients with chronic lymphocytic thyroiditis rapidly enlarging neck mass often is painless diagnosis usually is suggested by FNA biopsy, although needle-core or open biopsy may be necessary for definitive diagnosis
Lymphoma
Patients with thyroid lymphoma respond rapidly to chemotherapy (CHOP cyclophosphamide, doxorubicin, vincristine, and prednisone), which is also associated with improved survival. overall 5-year survival rate is about 50%
Thank You...