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Introduction And Importance: Intracranial dermoid cysts are rare benign tumors that originate from abnormal ectodermal cells containing epidermal features. Depending on the size and location of the lesion, these tumors can be asymptomatic or cause focal neurological deficits. This study describes a rare case of intraosseous parietal intracranial dermoid.
Case Presentation: A 25-year-old patient presented to the hospital with left hemiplegia and dysarthria. Furthermore, the investigation showed a large intracranial lesion. After establishing the diagnosis of the dermoid cyst, surgical resection was performed, and the diagnosis was affirmed by histology. The patient's follow-up period showed no recurrence.
Clinical Discussion: Dermoid cysts are benign tumors that are usually found in the midline. Parietal lesions are considered rare as well as intraosseous types of these lesions. Magnetic resonance imaging and computed tomography are essential for diagnosis and accurate therapy planning. Complete surgical resection is the treatment of choice in such cases.
Conclusion: Intraosseous parietal dermoid cysts are unusual lesions. Diagnosis is determined by clinical examination, imaging techniques, and microscopic examination. Surgery is considered crucial to avoid intracranial complications.
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http://dx.doi.org/10.1097/MS9.0000000000003384 | DOI Listing |
Case Rep Dent
August 2025
Department of Neurosciences-Dentistry Section, Padova University, Padova, Italy.
The aim of the study is to present a case of a dermoid cyst in the oral floor of an 80-year-old female patient and discuss its clinical presentation, diagnostic approach, and treatment. A retrospective case study was conducted at the Department of Maxillofacial Surgery, Aulss 2 Marca Trevigiana. The patient, with a medical history of hypertension, presented with a swelling in the oral floor.
View Article and Find Full Text PDFOrbit
September 2025
Department of Ophthalmology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Ann Med Surg (Lond)
September 2025
Department of Pathology, Nepal Medical College and Teaching Hospital, Kathmandu University, Nepal.
Introduction: Simultaneous presentation of acute appendicitis and ovarian torsion is rare and requires urgent surgical intervention due to the high risk of complications, including sepsis and mortality. While adnexal torsion is a known cause of acute abdomen in reproductive-age women, co-presentation with appendicitis is exceptionally uncommon. This case underlines the importance of considering gynecological differentials in women presenting with acute abdominal pain.
View Article and Find Full Text PDFAm J Case Rep
September 2025
Department of Urology, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou, Jiangsu, China.
BACKGROUND Primary retroperitoneal tumors (PRTs) are uncommon, with retroperitoneal dermoid cysts being particularly rare. The cystic cavity of mature cystic teratomas (dermoid cysts) is lined with squamous epithelium and primarily filled with sebaceous material. These lesions often lack specific symptoms, leading to delayed diagnosis.
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November 2025
Department of Radiology, Shaukat Khanum Memorial Cancer Hospital and Research Center, Lahore, Pakistan.
Mature cystic teratomas (MCTs) are common ovarian neoplasms that rarely undergo malignant transformation, particularly in pediatric patients. We report a rare case of a 5-year-old girl presenting with abdominal distension and back pain, initially managed with incomplete excision of an ovarian mass without histopathological evaluation. Recurrence led to debulking surgery revealing a mixed germ cell tumor, and subsequent imaging identified a residual abdominopelvic mass with elevated alpha-fetoprotein levels.
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