Deck 20: Bones, Joints, and Soft Tissue Tumors
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Deck 20: Bones, Joints, and Soft Tissue Tumors
1
Osteoid osteoma is a small benign bone tumor associated with pain that is disproportionate to the size of the lesion. This pain is caused by an excess of which of the following substances?
A) Interleukin (IL)-1 and IL-6
B) Leukotrienes
C) Prostaglandin E2
D) Complement C3
E) Bradykinin
A) Interleukin (IL)-1 and IL-6
B) Leukotrienes
C) Prostaglandin E2
D) Complement C3
E) Bradykinin
Prostaglandin E2
2
Loss of heterozygosity, structural rearrangements, or point mutations of the retinoblastoma tumor suppressor gene (RB) are found in 60%-70% of all sporadic bone tumors. Which of the following is the best classification for this tumor?
A) Osteosarcoma
B) Osteoblastoma
C) Osteoid osteoma
D) Chondrosarcoma
E) Ewing sarcoma
A) Osteosarcoma
B) Osteoblastoma
C) Osteoid osteoma
D) Chondrosarcoma
E) Ewing sarcoma
Osteosarcoma
3
The autosomal dominant bone disorder caused by a mutation of fibroblast growth factor receptor 3 (FGFR3) is characterized by short stature, rhizomelic shortening of limbs, frontal bossing of the skull, and midface abnormalities. Which of the following disorders is described by these characteristics?
A) Achondrogenesis
B) Achondroplasia
C) Multiple epiphyseal dysplasia
D) Synpolydactyly
E) Holt-Oram syndrome
A) Achondrogenesis
B) Achondroplasia
C) Multiple epiphyseal dysplasia
D) Synpolydactyly
E) Holt-Oram syndrome
Achondroplasia
4
Compression fractures of vertebral bodies seen in elderly women are causally related to reduced recruitment of osteoclasts. This process is associated with an increased concentration of which chemical mediators in the bone? 
A) Prostaglandins
B) Leukotrienes
C) Cytokines such as interleukin (IL)-1 and IL-6
D) Oncogenes such as c-MYC and K-RAS
E) Fibroblast growth factors

A) Prostaglandins
B) Leukotrienes
C) Cytokines such as interleukin (IL)-1 and IL-6
D) Oncogenes such as c-MYC and K-RAS
E) Fibroblast growth factors
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5
Trinucleotide CTG repeat expansion plays a role in the pathogenesis of which of the following muscle diseases?
A) Duchenne muscular dystrophy
B) Becker muscular dystrophy
C) Autosomal dominant limb girdle muscular dystrophy
D) Autosomal recessive limb girdle muscular dystrophy
E) Myotonic dystrophy
A) Duchenne muscular dystrophy
B) Becker muscular dystrophy
C) Autosomal dominant limb girdle muscular dystrophy
D) Autosomal recessive limb girdle muscular dystrophy
E) Myotonic dystrophy
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6
A 20-year-old man is being treated for a soft tissue tumor of the lower extremity. The tumor is composed of malignant spindle-shaped cells and epithelial cells that form gland-like structures. Which of the following is the most likely diagnosis?
A) Leiomyosarcoma
B) Malignant fibrous histiocytoma
C) Primitive neuroectodermal tumor
D) Synovial sarcoma
E) Rhabdomyosarcoma
A) Leiomyosarcoma
B) Malignant fibrous histiocytoma
C) Primitive neuroectodermal tumor
D) Synovial sarcoma
E) Rhabdomyosarcoma
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7
The primitive neuroectodermal tumor (PNET) of soft tissues has the same histologic features and the same chromosomal translocation as which of the following bone tumors?
A) Osteosarcoma
B) Chondrosarcoma
C) Ewing sarcoma
D) Malignant fibrous histiocytoma
E) Giant cell tumor of bones
A) Osteosarcoma
B) Chondrosarcoma
C) Ewing sarcoma
D) Malignant fibrous histiocytoma
E) Giant cell tumor of bones
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8
Which of the following muscle diseases is classified as an ion channel myopathy (channelopathy)?
A) Dysferlin deficiency
B) Becker muscular dystrophy
C) Malignant hyperpyrexia
D) Central core disease
E) Myotubular myopathy
A) Dysferlin deficiency
B) Becker muscular dystrophy
C) Malignant hyperpyrexia
D) Central core disease
E) Myotubular myopathy
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