An irregular outline, a thin wall, and the lack of erythrocytes in the lumen characterize lymphatic vessel. Arterioles (choices A and B) have thicker walls and contain erythrocytes. Venules (choice D) are thin-walled but they contain erythrocytes. Capillaries (choice E) are small in diameter and they contain erythrocytes.

41) A 4-month-old male infant is brought to the clinic because of excessive noisy respiration. On examination, the infant is within the normal range of growth, appears healthy, and does not show respiratory distress. Phonation is normal, along with head and neck examination findings. However, the child displays stridor (highpitched breathing sound) on inspiration, accentuated in the supine position. The parents report that the same stridor is heard during feeding or when the child is agitated. The attending physician places the child in the prone position and the stridor is relieved. To confirm, she holds the child in a neck extended position, which also relieves the stridor. An endoscopic laryngeal examination reveals bulky arytenoids cartilages and the diagnosis of laryngomalacia is established. During development, the arytenoids cartilages arise from which of the following?

The arytenoid cartilages arise as swellings from the sixth pharyngeal (branchial) arch at 32 days of gestation. They are located between the caudal end of the hypobranchial eminence and the cranial end of the laryngotracheal tube. The swellings will grow cranially to form the arytenoids and corniculate cartilages along with the primitive aryepiglottic folds. In laryngomalacia, the bulky arytenoid cartilages prolapse anteromedially on inspiration, resulting in stridor. The first (choice A), second (choice B), and third (choice C) pharyngeal arches do not participate in the development of laryngeal cartilages. The fifth (choice D) pharyngeal arch remains rudimentary and does not give rise to any adult structure.

42) An 8-year-old male patient is brought to a rural hospital with a history of recurrent infection. The patient has a characteristic facies with a high, broad nasal bridge, long face, narrow palpebral fissures, and an abnormally small mandible. The patient also has a cleft palate. The patient is diagnosed with DiGeorge syndrome, an inherited immunodeficiency disease due to a chromosome 22q11.2 deletion. In this syndrome, the production of which of the following cells is affected in the thymus?

In DiGeorge syndrome, the cortical epithelial cells of the thymus fail to develop and the thymus is hypoplastic. As a result, bone marrow-derived T-cell precursors cannot differentiate and functional T-cell production is markedly reduced. The development of B cells (choice A) is not affected in DiGeorge syndrome. Endothelial cells (choice B) forming the vascular walls are not affected by thymic maldevelopment, nor are the cells of myeloid lineage, the macrophages (choice C), and the neutrophils (choice D).

In TGA, the aorta arises from the right ventricle and the pulmonary trunk arises from the left ventricle (choice C). This is the reverse of the normal situation and gives rise to the cyanotic condition in the newborn. The large arteries arise from the truncus arteriosus in the developing heart and thus could not develop from the atria (choices B and D), which are formed from the sinus venosus. The truncus arteriosus and the sinus venosus are at opposite ends of the heart. The ductus arteriosus (choice A) is the vessel that shunts oxygenated blood from the pulmonary trunk to the arch of the aorta in the fetus. It does not give rise to the aorta.

An irregular outline, a thin wall, and the lack of erythrocytes in the lumen characterize lymphatic vessel. Arterioles (choices A and B) have thicker walls and contain erythrocytes. Venules (choice D) are thin-walled but they contain erythrocytes. Capillaries (choice E) are small in diameter and they contain erythrocytes.

This is the secretory portion of the eccrine sweat gland, recognizable by its three cell types. The apical dark cells (arrow 1) are closest to the lumen. The clear or basal cells (arrow 2) and the myoepithelial cells (arrow 3) are located against the basal lamina. Characteristically, these cells are large and the lumen is small. The apocrine sweat gland (choice A) is lined with simple cuboidal epithelium and thus has a large lumen. The dermal papilla (choice B) is formed by fibroblasts, not epithelia. The hair follicle (choice D) is formed by three concentric zones of keratinized cells and does not have a lumen. The sebaceous glands (choice E) are appendages of the hair follicle and their lumen is lined by stratified squamous epithelium.

The posterior inferior cerebellar artery supplies the rostral, dorsolateral medulla. The posterior spinal (choice D) and anterior spinal (choice B) arteries supply dorsal and ventral portions, respectively, of the caudal medulla. The anterior inferior cerebellar (choice A) and superior cerebellar (choice E) arteries supply portions of the pons and mesencephalon.

Arrow 2 points to the abdominal aorta, located anterior to the lumbar vertebra. Arrows 1 (choice A) and 5 (choice B) indicate the left and right kidneys respectively. Arrow 3 points to the inferior vena cava; the junctions of the left and right renal veins to the inferior vena cava are seen in this CT scan. Arrow 4 points to a loop of the small intestine, filled with contrastenhancing material.

Arrow 2 points to the base of the gastric glands where chief or peptic (zymogenic) cells tend to be clustered. Arrow 1 points to the luminal surface of the stomach where mucus-secreting cells are found. Arrow 3 points to the muscularis mucosae. Arrow 4 points to the middle of the gastric glands where parietal or oxyntic cells tend to be most numerous. Arrow 5 point to the side of a gastric pit where mucus-secreting cells are also found.

49) A 62-year-old patient diagnosed with prostate carcinoma complains of a right-sided headache worsening over 4 days and displays a drooping right upper eyelid. Examination reveals a right third nerve palsy. An MRI reveals a single metastasis of the prostatic carcinoma in the right side of the midbrain, causing Benedikt’s syndrome. Which of the following signs would also be seen in this patient?