100 Examples of sentences containing the common noun "rhabdomyoma"

Definition

Rhabdomyoma is a rare benign tumor of striated muscle tissue, typically found in the heart (cardiac rhabdomyoma) or skeletal muscles. It is often associated with certain genetic conditions, such as tuberous sclerosis.

Synonyms

• Muscle tumor
• Striated muscle tumor

Antonyms

• Rhabdomyosarcoma (a malignant counterpart)

Examples

1. The doctor diagnosed the patient with Rhabdomyoma after reviewing the ultrasound results.
2. In pediatric cases, Rhabdomyoma can often be linked to underlying genetic disorders.
3. The presence of Rhabdomyoma in the heart can lead to arrhythmias.
4. Surgical removal of Rhabdomyoma is sometimes necessary if it obstructs cardiac function.
5. Researchers are studying the molecular pathways that lead to Rhabdomyoma development.
6. The symptoms of Rhabdomyoma can vary depending on its location in the body.
7. Due to its benign nature, Rhabdomyoma usually has a good prognosis.
8. A biopsy confirmed the diagnosis of Rhabdomyoma in the skeletal muscle.
9. The child’s frequent fainting spells were attributed to a Rhabdomyoma in the heart.
10. As Rhabdomyoma can be asymptomatic, regular check-ups are crucial for early detection.
11. The cardiologist explained that Rhabdomyoma is often mistaken for other heart conditions.
12. Imaging studies revealed the presence of Rhabdomyoma in the patient’s left ventricle.
13. Genetic counseling is recommended for families with a history of Rhabdomyoma.
14. The likelihood of developing Rhabdomyoma increases in individuals with tuberous sclerosis.
15. Researchers are exploring the genetic mutations associated with Rhabdomyoma.
16. The surgical team prepared for the removal of a Rhabdomyoma located near the diaphragm.
17. The symptoms related to Rhabdomyoma can be similar to those of other muscle disorders.
18. The prenatal ultrasound detected a Rhabdomyoma, raising concerns for the parents.
19. After the excision of the Rhabdomyoma, the patient showed significant improvement.
20. The pathologist confirmed the tumor was a Rhabdomyoma through microscopic examination.
21. The rarity of Rhabdomyoma makes it a subject of interest in medical research.
22. Follow-up appointments are essential after the diagnosis of Rhabdomyoma.
23. The healthcare team monitored the child for any signs of complications from the Rhabdomyoma.
24. The patient experienced chest pain, which led to the discovery of a Rhabdomyoma.
25. Rhabdomyoma can occur in various muscle tissues, though it is most common in the heart.
26. Clinical trials are underway to better understand the treatment options for Rhabdomyoma.
27. The presence of Rhabdomyoma in the heart can be detected through echocardiography.
28. The prognosis for patients with Rhabdomyoma is generally favorable.
29. The multidisciplinary team discussed the best approach to manage the Rhabdomyoma.
30. A follow-up MRI was scheduled to monitor the Rhabdomyoma for any changes.
31. The genetic basis of Rhabdomyoma is being investigated in several studies.
32. The child was referred to a specialist after the detection of a Rhabdomyoma.
33. The doctor explained that Rhabdomyoma could sometimes resolve on its own.
34. The patient was relieved to learn that Rhabdomyoma is not cancerous.
35. A family history of Rhabdomyoma raised suspicions for genetic testing.
36. The surgery to remove the Rhabdomyoma was successful and well-tolerated.
37. The pediatrician explained that Rhabdomyoma is often discovered incidentally.
38. The association between Rhabdomyoma and tuberous sclerosis is well-documented.
39. After the diagnosis of Rhabdomyoma, the family received support from patient advocacy groups.
40. The cardiologist noted that Rhabdomyoma can cause obstruction in heart chambers.
41. The team prepared for the delicate procedure to excise the Rhabdomyoma.
42. Rhabdomyoma can lead to complications if left untreated.
43. The patient's symptoms improved significantly after the removal of the Rhabdomyoma.
44. A thorough evaluation is needed to assess the impact of Rhabdomyoma on health.
45. The awareness of Rhabdomyoma among healthcare professionals is crucial for early diagnosis.
46. The rare nature of Rhabdomyoma means that many doctors may not encounter it frequently.
47. The research team published findings on the genetic markers of Rhabdomyoma.
48. The patient’s family was educated about the nature of Rhabdomyoma and its implications.
49. The echocardiogram revealed a sizable Rhabdomyoma in the left atrium.
50. The rarity of Rhabdomyoma makes it a fascinating topic for medical case studies.
51. Rhabdomyoma can sometimes mimic other types of tumors during diagnosis.
52. The discovery of Rhabdomyoma during routine imaging was unexpected.
53. The medical team discussed the potential need for further intervention if the Rhabdomyoma grew.
54. The possibility of Rhabdomyoma recurrence is low after surgical removal.
55. The significance of regular screening for Rhabdomyoma in high-risk populations cannot be overstated.
56. The long-term outcomes for patients with Rhabdomyoma are generally positive.
57. The patient's case of Rhabdomyoma was presented at a medical conference for further insights.
58. The genetic predisposition to Rhabdomyoma was highlighted in the family’s medical history.
59. The surgical approach to Rhabdomyoma varies based on its location and size.
60. The risks associated with a Rhabdomyoma depend on its specific characteristics.
61. The medical literature outlines several case studies involving Rhabdomyoma.
62. Rhabdomyoma can usually be differentiated from malignant tumors through imaging and biopsy.
63. The interdisciplinary team's strategy to address the Rhabdomyoma included both medical and surgical options.
64. The benign nature of Rhabdomyoma is often a relief to patients and their families.
65. The finding of a Rhabdomyoma was a surprise during the routine check-up.
66. The patient was advised to monitor any symptoms related to their Rhabdomyoma.
67. The impact of Rhabdomyoma on the patient’s quality of life was discussed during the consultation.
68. The healthcare provider reassured the family that Rhabdomyoma is treatable.
69. The presence of Rhabdomyoma is an important consideration in pediatric cardiology.
70. Rhabdomyoma can often be asymptomatic, complicating early diagnosis.
71. The research focused on the biochemical markers that could indicate Rhabdomyoma presence.
72. The potential for developing Rhabdomyoma later in life is a concern for those with a family history.
73. The medical team assessed the implications of the Rhabdomyoma on the patient's overall health.
74. The child’s Rhabdomyoma was monitored over several months to assess growth.
75. The healthcare system is working on improving the diagnostic criteria for Rhabdomyoma.
76. The patient expressed relief at learning that Rhabdomyoma is benign.
77. The complexity of Rhabdomyoma cases often requires a collaborative approach to treatment.
78. The findings related to Rhabdomyoma have led to advancements in treatment protocols.
79. The multidisciplinary team provided comprehensive care for the patient with Rhabdomyoma.
80. The prognosis for individuals with Rhabdomyoma is generally optimistic.
81. The implications of a Rhabdomyoma diagnosis can vary significantly among patients.
82. Rhabdomyoma research continues to evolve as new genetic insights emerge.
83. The surgical intervention for Rhabdomyoma was deemed necessary for the patient’s health.
84. The family was educated about potential symptoms of Rhabdomyoma to watch for.
85. The team of specialists worked together to address the Rhabdomyoma effectively.
86. The importance of early detection of Rhabdomyoma cannot be overlooked.
87. The pediatric team discussed the implications of Rhabdomyoma with the parents.
88. The child's athletic ability was not significantly affected by the Rhabdomyoma.
89. The clinic specializes in the management of rare tumors like Rhabdomyoma.
90. The literature review highlighted the rarity of Rhabdomyoma in adults.
91. The impact of a Rhabdomyoma on cardiac function was a major concern for the cardiologist.
92. The detection of Rhabdomyoma in utero raised several medical questions for the team.
93. The patient’s follow-up appointments focused on monitoring the Rhabdomyoma.
94. The presence of a Rhabdomyoma can complicate standard treatment protocols.
95. The case report on the patient with Rhabdomyoma provided valuable insights for clinicians.
96. The long-term effects of Rhabdomyoma are still being researched.
97. Genetic testing revealed a predisposition to Rhabdomyoma in the family.
98. The treatment plan for Rhabdomyoma was tailored to the patient’s specific needs.
99. The role of imaging in diagnosing Rhabdomyoma is crucial for accurate assessment.
100. The support group for patients with Rhabdomyoma helped the family cope with the diagnosis.