Intracranial teratoma, a subtype of non-germinomatous germ cell tumors, is rare in adults. Clinical presentation of intracranial teratomas varies according to where they grow. In particular, cases of spontaneous ruptures of intracranial teratoma are sporadic. This study reports the case of an adult with a spontaneously ruptured mature teratoma in the cerebellar vermis, which was comorbid with a dermal sinus tract and subcutaneous lipoma. Before surgery, because the images were atypical of a teratoma, the patient was misdiagnosed as having vascular malformation rupture and bleeding in the cerebellar vermis. Due to the patient's level of consciousness dropping drastically to a coma, a craniotomy was performed. During the surgery, the tumor was observed to be a mixed cystic and solid mass. The liquid in the cyst was dark green and with a fatty component. The solid part had a tough texture and comprised hair, fat, cartilage, and calcification components. Post-surgery multipoint biopsy proved that it was a mature teratoma and that it was connected to a subcutaneous lipoma through the dermal sinus tract across the occipital bone. After proactive treatment, the patient's prognosis was favorable.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11417044 | PMC |
http://dx.doi.org/10.7759/cureus.67634 | DOI Listing |
Pathol Res Pract
December 2024
IIND Department of Gynecological Oncology and Gynecological Surgery, Lublin Medical University, Lublin, Poland. Electronic address:
Although mature ovarian teratoma (MOT) is one of the most commonly detected benign tumours worldwide, its malignant transformation is rare. This article presents a case of a 47-year-old woman, operated on for emergency reasons due to a giant painful ovarian tumour, showing preoperatively no signs of malignancy. Surprisingly, a pathological report showed MOT coexisting with an early-stage ovarian adenocarcinoma developing as an endophytic papilloma.
View Article and Find Full Text PDFChilds Nerv Syst
January 2025
Division of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Purpose: We sought to evaluate the incidence, natural history, and management of cystic spinal lesions following myelomeningocele/myeloschisis closure.
Methods: We performed a single-center retrospective review of all patients who underwent myelomeningocele/myeloschisis closure from 2013 to 2018 with follow-up to 5 years old.
Results: We analyzed 100 fetal repairs and 81 postnatal closures from 305 total surgeries.
Introduction: We present a rare case of long-term survival following metastasectomy for lumbar metastasis with growing teratoma syndrome.
Case Presentation: An 18-year-old man presented with left scrotal mass and lumbago. Alpha-fetoprotein was elevated to 648.
J Minim Invasive Gynecol
December 2024
Department of Gynecology, The Second People's Hospital of Guiyang, Guiyang, China.
Fetiform teratoma, another name for homunculus, is a rare form of mature teratoma that is highly differentiated and has parts that resemble a malformed fetus. We reported a case of ovarian Fetiform teratoma in a 38 years old nulliparous woman presented with right side abdominal distention of 10 years duration. An ultrasound revealed a heterogeneous pelvic cystic mass that ranged in appearance from fully hyperechoic to fully hypoechoic, suggesting mature cystic teratoma.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!