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1.
Ann R Coll Surg Engl ; 102(1): e1-e3, 2020 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-31155921

RESUMO

Diffuse cavernous haemangioma is a rare disease of the rectum. It usually presents with a history of rectal bleeding in children and young adults. When conservative methods fail to control bleeding, traditionally resection is recommended. A 50-year-old man presented with per rectal bleeding and was diagnosed with diffuse cavernous haemangioma of the sigmoid and rectum extending up to 40 cm in the left colon through endoscopy, magnetic resonance imaging and computed tomography. The diagnosis was confirmed by biopsy. This patient was successful managed conservatively with tranexamic acid as needed, avoiding the need for resection.


Assuntos
Antifibrinolíticos/administração & dosagem , Tratamento Conservador/métodos , Hemangioma Cavernoso/tratamento farmacológico , Neoplasias Retais/tratamento farmacológico , Neoplasias do Colo Sigmoide/tratamento farmacológico , Ácido Tranexâmico/administração & dosagem , Administração Oral , Colonoscopia , Hemorragia Gastrointestinal/etiologia , Hemangioma Cavernoso/diagnóstico , Humanos , Imagem por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Imagem Multimodal , Neoplasias Retais/diagnóstico , Neoplasias do Colo Sigmoide/diagnóstico , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Conduta Expectante
2.
J Cardiothorac Surg ; 14(1): 199, 2019 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-31730003

RESUMO

BACKGROUND: Cardiac cavernous hemangiomas are extremely rare and usually difficult to be diagnosed for being asymptomatic. CASE PRESENTATION: An asymptomatic 56-year-old woman was hospitalized due to a heart mass found by chest computed tomography (CT) during her annual physical examination. Coronary computed tomography angiography (CTA) disclosed a tumorous lesion, located in the left atrial roof and extended to the posterior wall of the aortic root and surrounding the left main coronary artery. However, there was no communicating branches between the hemangioma and coronary artery and no coronary artery stenosis. The tumor was excised with low-frequency electrocautery under cardiopulmonary bypass. The histopathological examination indicated the mass a cavernous hemangioma. The patient was discharged with an uneventful recovery. CONCLUSIONS: Here we presented a rare case of successfully excision of a cavernous hemangioma involving the left atrial roof and left coronary artery. We advocate adequate exposure and complete surgical excision with low-frequency electrocautery to avoid remnants and excessive resection.


Assuntos
Procedimentos Cirúrgicos Cardíacos/métodos , Neoplasias Cardíacas/diagnóstico , Hemangioma Cavernoso/diagnóstico , Tomografia Computadorizada por Raios X/métodos , Fibrilação Atrial , Feminino , Átrios do Coração , Neoplasias Cardíacas/cirurgia , Hemangioma Cavernoso/cirurgia , Humanos , Pessoa de Meia-Idade
3.
Clin Lab ; 65(9)2019 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-31532104

RESUMO

BACKGROUND: The Cavernous Angioma in Posterior Sagittal Sinus is exceedingly rare. METHODS: We report for the case of a 10-year-old male patient who was diagnosed with Cavernous Angioma in Posterior Sagittal Sinus. RESULTS: Our case is the second reported case of Cavernous Angioma in Posterior Sagittal Sinus in the world. CONCLUSIONS: It is very rare for the cavernous hemangioma to occur in the sinus, preoperative conventional MR scan lacks specificity and easily leads to misdiagnosis. Head MR enhancement, MRBTI, and SWI can provide more useful diagnostic information. The final diagnosis depends on the pathology examination.


Assuntos
Seio Cavernoso/patologia , Dura-Máter/irrigação sanguínea , Hemangioma Cavernoso/diagnóstico , Neoplasias Meníngeas/diagnóstico , Seio Cavernoso/diagnóstico por imagem , Criança , Dura-Máter/diagnóstico por imagem , Hemangioma Cavernoso/diagnóstico por imagem , Humanos , Imagem por Ressonância Magnética/métodos , Masculino , Neoplasias Meníngeas/diagnóstico por imagem , Tomografia Computadorizada por Raios X/métodos
4.
Technol Cancer Res Treat ; 18: 1533033819876981, 2019 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-31530156

RESUMO

OBJECTIVE: To evaluate the efficacy and safety of hypofractionated stereotactic radiotherapy using CyberKnife for high volume cavernous sinus cavernous hemangiomas. MATERIALS AND METHODS: We collected data from 12 patients with high volume cavernous sinus cavernous hemangiomas treated with hypofractionated stereotactic radiotherapy using CyberKnife in our institute, including 2 men and 10 women/female child, aged 4 to 60 years. Initial tumor volumes ranged from 11.8 to 96.6 cm3 with a median of 24.3 cm3. Irradiation doses were 19.5 Gy with 3 fractions in 2 patients, 21 Gy with 3 fractions in 8 patients, 25 Gy with 5 fractions in 1 patient, and 30 Gy with 3 fractions in 1 patient. We used 109 to 155 beams during treatment, and target volumes reached over 95% of the prescribed dose. Follow-up ranged from 3 to 54 months. We evaluated the efficacy and safety of the CyberKnife system based on changes in the diagnostic images and involved cranial nerves or symptoms. RESULTS: Of the 12 patients, 11 were followed for 3 to 54 months with a mean follow-up of 16.3 months; 1 patient was lost to in-person follow-up. Lesion volumes in the followed 11 patients were calculated after fractionated radiotherapy. All tumor volumes decreased (28.6%-94.1%) and symptoms improved (including blurred vision, visual field defects, diplopia, headaches, and facial numbness) after therapy. Postoperative magnetic resonance images revealed a tumor volume range of 2.8 to 41.0 cm3 (median, 6.5 cm3), significantly lower compared with the pretreatment range of 11.8 to 70.1 cm3 (median, 24.3 cm3; T = 0.00, P = .003 < .05). A single patient experienced radiotherapy-related cerebral edema, which resolved after 5 days of mannitol and dexamethasone. CONCLUSIONS: Based on the current results, though preliminary, hypofractionated stereotactic radiotherapy using CyberKnife is an effective and safe alternative for high volume cavernous sinus cavernous hemangiomas and is the recommended primary treatment in high-risk patients with this condition.


Assuntos
Hemangioma Cavernoso/radioterapia , Hipofracionamento da Dose de Radiação , Radiocirurgia , Adolescente , Adulto , Criança , Pré-Escolar , Gerenciamento Clínico , Feminino , Hemangioma Cavernoso/diagnóstico , Humanos , Imagem por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Radiocirurgia/métodos , Dosagem Radioterapêutica , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Adulto Jovem
5.
J Craniofac Surg ; 30(7): e681-e683, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31449226

RESUMO

Intraosseous hemangioma (IH) in the maxillofacial area is a very uncommon neoplasm. Here, the authors show an exceptional case not previously reported in the literature of a 65-year-old man who presented with a pathological mandibular fracture following a facial trauma that was the first sign of an occult cavernous IH. Complete excision of the tumor in the mandibular ramus reduced the risk of severe bleeding and prevented long-term recurrence, whereas immobilization of the fracture obtained an excellent functional result. This clinical report highlights the possibility that a previously unknown primary IH may debut as a pathological fracture and the importance of differential diagnosis in this location.


Assuntos
Diagnóstico Diferencial , Fraturas Espontâneas/diagnóstico por imagem , Hemangioma Cavernoso/diagnóstico , Fraturas Mandibulares/diagnóstico por imagem , Idoso , Fraturas Espontâneas/cirurgia , Humanos , Masculino , Fraturas Mandibulares/cirurgia , Recidiva Local de Neoplasia/diagnóstico
6.
World Neurosurg ; 130: 298-303, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31306838

RESUMO

BACKGROUND: A 61-year-old man was admitted complaining of myelopathy and back pain for 3 months. CASE DESCRIPTION: A 15-mm hemangioma with calcification was noted on magnetic resonance imaging and computed tomography. Intraoperatively, the mass was hard with ill-defined demarcation. The cranial portion of the mass was brown and dark gray on the dorsal cord. During surgery, motor evoked potentials transiently decreased, but they fully recovered at the end of surgery. After surgery, the patient's symptoms recovered without severe neurologic deficit. CONCLUSIONS: Hemangioma calcificans, a variant of cavernous hemangioma with full calcification and ossification, is an extremely rare disease in the spine and brain. Here we report a rare case of intramedullary cavernous hemangioma with calcification of the spinal cord.


Assuntos
Calcinose/patologia , Hemangioma Cavernoso/cirurgia , Neoplasias da Medula Espinal/cirurgia , Medula Espinal/cirurgia , Calcinose/diagnóstico , Potencial Evocado Motor/fisiologia , Hemangioma Cavernoso/diagnóstico , Humanos , Masculino , Pessoa de Meia-Idade , Medula Espinal/patologia , Neoplasias da Medula Espinal/diagnóstico , Coluna Vertebral/patologia , Tomografia Computadorizada por Raios X/métodos
7.
J Clin Neurosci ; 67: 272-275, 2019 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-31221581

RESUMO

PURPOSE: Orbital haemangiomas are common orbital tumors known for their slow growth. Acute presentation with haemorrhage into the tumor is a rare occurrence with only nine cases reported in literature. METHODS: The authors present a case of an elderly female with sudden onset of proptosis and swelling of the eye. There was a transient relief of symptoms with steroids with residual proptosis and ptosis at two weeks. Magnetic resonance imaging revealed an intraconal soft tissue mass in the inferolateral quadrant of the left orbit with a differential diagnosis of haemangioma with bleed or metastasis. RESULTS: Patient underwent a lateral orbitotomy and tumour excision and histopathological examination revealed a cavernous haemangioma with a thrombus. The patient had complete symptomatic recovery following surgery. CONCLUSION: Orbital haemangiomas presenting with haemorrhage is rare and should be differentiated from orbital venous anomalies prior to surgery.


Assuntos
Hemangioma Cavernoso/diagnóstico , Hemorragia/diagnóstico , Neoplasias Orbitárias/diagnóstico , Idoso , Diagnóstico Diferencial , Feminino , Hemangioma Cavernoso/complicações , Hemangioma Cavernoso/cirurgia , Hemorragia/etiologia , Hemorragia/cirurgia , Humanos , Neoplasias Orbitárias/complicações , Neoplasias Orbitárias/cirurgia
8.
Rozhl Chir ; 98(4): 178-180, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31159552

RESUMO

Cavernous hemangiomas are benign tumours of mesodermal origin. Even though various localizations of hemangioma have been described in the literature, its occurrence in the greater omentum is very rare. Only symptomatic hemangiomas are indicated for surgical treatment. There are case reports presenting resection or surgical removal of the greater omentum with hemangioma because of mechanical syndrome, consumption coagulopathy, bleeding, infection or suspicion of a malignancy. This article presents a case report of a patient operated on for a suspicion of carcinomatosis of the greater omentum. Histological examination found hemangiomatosis in the resected greater omentum.


Assuntos
Hemangioma Cavernoso , Hemangioma Cavernoso/diagnóstico , Hemangioma Cavernoso/cirurgia , Hemorragia , Humanos , Omento
9.
J Cardiothorac Surg ; 14(1): 95, 2019 May 22.
Artigo em Inglês | MEDLINE | ID: mdl-31118062

RESUMO

BACKGROUND: Cavernous hemangioma of the rib is extremely rare benign vascular tumor. It is difficult to diagnose in time because both invasive and noninvasive examinations usually fail to distinguish it from other tumors of the rib and other bones. CASE PRESENTATION: We described an asymptomatic 44-year-old woman with cavernous hemangioma of the rib that was incidentally discovered in the bathing. The tumor was completely resected by minithoracotomy through posterolateral incision. The pathological tissue was diagnosed as a cavernous hemangioma composed of thin-walled blood vessels and red blood cells. CONCLUSIONS: We reported this case of giant cavernous hemangioma of the rib for its extremely rare occurrence. The preoperative diagnosis is a challenge both clinically and radiologically, and difficult to distinguish this tumor from other tumors of the rib or long bones.


Assuntos
Neoplasias Ósseas/diagnóstico , Hemangioma Cavernoso/diagnóstico , Costelas/cirurgia , Adulto , Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/cirurgia , Diagnóstico Diferencial , Feminino , Hemangioma Cavernoso/diagnóstico por imagem , Hemangioma Cavernoso/cirurgia , Humanos , Toracotomia , Tomografia Computadorizada por Raios X
10.
Indian J Ophthalmol ; 67(4): 561-563, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30900601

RESUMO

Retinal cavernous hemangiomas is a rare vascular tumor, isolated and non-progressive. This tumor is incidentally diagnosed on fundus examination and visual impairment can be rare presentation from vitreous hemorrhage, pre-retinal traction, hyphema, or macular scarring. The tumor has typical appearance of grape-like clusters of dilated vascular sacs with variable surface gliosis. Characteristic imaging findings aids in diagnosis. Newly emerged imaging tool is optical coherence tomography angiography (OCT A) which obtains high-resolution visualization of retinal vasculature in non-invasive fashion. In the present case report, we analyzed various diagnostic tool available for retinal cavernous hemangiomas; illustrating on the OCT A features.


Assuntos
Angiofluoresceinografia/métodos , Hemangioma Cavernoso/diagnóstico , Retina/patologia , Neoplasias da Retina/diagnóstico , Tomografia de Coerência Óptica/métodos , Feminino , Fundo de Olho , Humanos , Pessoa de Meia-Idade
11.
BMC Cancer ; 19(1): 172, 2019 Feb 25.
Artigo em Inglês | MEDLINE | ID: mdl-30803439

RESUMO

BACKGROUND: Primary intraosseous cavernous hemangiomas (PICHs) of the skull are extremely rare. To date, diffuse cranial hemangioma of skull has not been reported. In cancer patients, it is often misdiagnosed as metastasis. CASE PRESENTATION: Here, we presented a case of a 50-year-old female patient suffering from slightly headache who received breast cancer modified radical mastectomy in 2004, computed tomography and magnetic resonance imaging findings revealed abnormal lesions of diffuse skull which were misdiagnosed as skull metastasis, and the relevant literatures were also reviewed. CONCLUSIONS: Diffuse cavernous hemangioma of the skull is exceedingly rare, and imaging data are not typical. The condition is often misdiagnosed, and pathological evaluation is necessary and important. In cases where the mass cannot be completely removed by surgery, radiotherapy could be beneficial.


Assuntos
Neoplasias da Mama/diagnóstico , Hemangioma Cavernoso/diagnóstico , Neoplasias Cranianas/diagnóstico , Crânio/patologia , Neoplasias da Mama/patologia , Diagnóstico Diferencial , Erros de Diagnóstico , Feminino , Hemangioma Cavernoso/patologia , Humanos , Imagem por Ressonância Magnética , Pessoa de Meia-Idade , Metástase Neoplásica , Crânio/diagnóstico por imagem , Neoplasias Cranianas/patologia , Tomografia Computadorizada por Raios X
12.
Fetal Pediatr Pathol ; 38(2): 175-181, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30676122

RESUMO

INTRODUCTION: Hepatic hemangiomas (HH) are benign vascular tumors, and when large, may contribute to fetal morbidity/mortality. Chorangiosis is placental villus capillary hypervascularity, probably linked with fetal hypoxia. CASE REPORT: We present a macrosomic stillbirth at 39 + 3 weeks of gestation with congestive heart failure (CHF) and myocardial infarction. A giant right hepatic lobe HH was present, along with placental chorangiosis. CONCLUSION: A common pathogenetic pathway between congenital HH and placental chorangiosis has not been reported. Our case suggests that the effects of HH and chorangiosis increase the risk of late fetal loss due to the high-output CHF.


Assuntos
Hemangioma/patologia , Neoplasias Hepáticas/patologia , Placenta/patologia , Natimorto/genética , Adulto , Vilosidades Coriônicas/patologia , Feminino , Hemangioma/diagnóstico , Hemangioma Cavernoso/diagnóstico , Hemangioma Cavernoso/patologia , Humanos , Fígado/patologia , Neoplasias Hepáticas/diagnóstico , Doenças Placentárias/diagnóstico , Doenças Placentárias/patologia , Gravidez
14.
Turk Patoloji Derg ; 35(1): 55-57, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-28272668

RESUMO

Primary cardiac tumors are rare in children with a low incidence varying from 0.0017 to 0.28% in autopsy studies. Approximately 90% of the reported primary cardiac tumors in the pediatric population are benign and the most common subtype is rhabdomyomas accounting for approximately 60%, while hemangiomas are rare primary tumors with a 5% incidence. Hypoplastic left heart syndrome is abnormal development of the left-sided cardiac structures, leading to obstruction of blood flow from the left ventricle out-flow tract. Here we report a case of tricuspid hemangioma in association with hypoplastic left heart syndrome, a rare association not previously reported in the literature.


Assuntos
Neoplasias Cardíacas/patologia , Hemangioma Cavernoso/patologia , Síndrome do Coração Esquerdo Hipoplásico/patologia , Morte Súbita do Lactente/etiologia , Feminino , Neoplasias Cardíacas/complicações , Neoplasias Cardíacas/diagnóstico , Hemangioma Cavernoso/complicações , Hemangioma Cavernoso/diagnóstico , Humanos , Síndrome do Coração Esquerdo Hipoplásico/complicações , Síndrome do Coração Esquerdo Hipoplásico/diagnóstico , Recém-Nascido , Morte Súbita do Lactente/diagnóstico , Morte Súbita do Lactente/patologia , Valva Tricúspide/patologia
15.
Medicine (Baltimore) ; 97(51): e13509, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30572451

RESUMO

RATIONALE: Cavernous hemangiomas are benign vascular malformations that usually involve the skin, subcutaneous tissue, and liver. Described herein was multiple masses in the lung and liver mimicking metastasis, which was proved to be cavernous hemangiomas histologically. PATIENT CONCERNS: A 78-year-old man with complaint of dizziness for 3 days was referred to the local hospital for medical attention. DIAGNOSES: Multiple masses in the lung and liver was diagnosed pathologically as cavernous hemangioma. INTERVENTIONS: Because of the benign pathological characteristic and multiple distribution, no treatment except some symptomatic treatment for dizziness was administered. OUTCOME: After more than 2 years of follow-up visits, the patient had no apparent symptoms and was healthy. LESSONS: Proper diagnosis of multiple cavernous hemangiomas is essential. The final diagnosis depends on the pathology results. The most appropriate management is follow-up. Surgical treatment is suitable for large or symptomatic lesions which can result in satisfactory prognoses.


Assuntos
Hemangioma Cavernoso/diagnóstico , Neoplasias Hepáticas/diagnóstico , Neoplasias Pulmonares/diagnóstico , Idoso , Diagnóstico Diferencial , Tontura/diagnóstico , Tontura/etiologia , Tontura/terapia , Hemangioma Cavernoso/complicações , Hemangioma Cavernoso/patologia , Humanos , Neoplasias Hepáticas/complicações , Neoplasias Hepáticas/patologia , Neoplasias Pulmonares/complicações , Neoplasias Pulmonares/patologia , Masculino
17.
An. sist. sanit. Navar ; 41(3): 381-385, sept.-dic. 2018. ilus
Artigo em Espanhol | IBECS | ID: ibc-179086

RESUMO

Los hemangiomas cavernosos representan menos del 1% de todos los tumores óseos, siendo las vértebras y el cráneo las localizaciones más habituales. Estos tumores son extremadamente raros en los huesos de la nariz, con muy pocos casos publicados en la literatura médica, descritos en cornetes, vómer, huesos propios o lamina erpendicular del etmoides. Suelen presentarse como una lesión tumoral que crece con el tiempo, implicando al hueso e incluso a tejidos blandos, pudiendo causar complicaciones como obstrucción nasal, sangrado, ulceraciones e infección, entre otras. Presentamos el caso de un paciente de 37 años con un hemangioma cavernoso localizado en los huesos propios de la nariz, revisándose los aspectos más destacados de este raro tumor


Cavernous hemangiomas represent less than 1% of all bone tumours, with the vertebrae and the skull being the most common locations. These tumours are extremely rare in the bones of the nose, with very few cases published in the medical literature, where they have been reported in turbinates, vomer, nasal bones or perpendicular lamina of the ethmoid. They usually present as a tumour lesion that grows over time, involving the bone and even the soft tissues, which can cause complications such as nasal obstruction, bleeding, ulcerations and infection. We present the case of a 37 year old patient with a cavernous hemangioma located in the bones of the nose, reviewing the most notable aspects of this rare tumour


Assuntos
Humanos , Masculino , Adulto , Hemangioma Cavernoso/diagnóstico , Hemangioma Cavernoso/cirurgia , Neoplasias Nasais/diagnóstico , Osso Nasal/cirurgia , Diagnóstico Diferencial , Neoplasias Nasais/patologia , Neoplasias Nasais/cirurgia , Osso Nasal/patologia
18.
BMC Surg ; 18(1): 103, 2018 Nov 20.
Artigo em Inglês | MEDLINE | ID: mdl-30458815

RESUMO

BACKGROUND: Adrenal cavernous hemangiomas are very rare benign tumors that usually present as incidental findings on abdominal imaging. Preoperative differential diagnosis from other benign or malignant adrenal neoplasms may be challenging. CASE PRESENTATION: A 70-year old man was referred for an 8-cm abdominal mass incidentally discovered on a contrast-enhanced computed tomography (CT) performed to investigate a pulmonary nodule. Biochemical tests ruled out any endocrine dysfunction and iodine 123 metaiodobenzylguanidine whole body scintiscan single-photon emission CT excluded a pheocromocitoma. Findings on magnetic resonance imaging were non-specific and the patient was elected for a left adrenalectomy. Histopathological diagnosis revealed a cavernous hemangioma. A portion of the resected tissue was tested for drug sensitivity to mitotane, doxorubicin, and sunitinib. CONCLUSIONS: Adrenal hemangioma is a rare disease but should be included in the differential diagnosis of adrenal tumors. The surgical resection is generally required to exclude malignant disease, resolve pressure-related symptoms, and prevent retroperitoneal hemorrhage. Although specific features in diagnostic imaging are often lacking, if the diagnosis is established preoperatively a laparoscopic adrenalectomy can be performed due to the benign nature of the lesion. Doxorubicin and sunitinib were both capable of reducing primary culture cell viability, this suggest that similar drugs may be useful in the medical treatment of adrenal hemangiomas.


Assuntos
Neoplasias das Glândulas Suprarrenais/diagnóstico , Adrenalectomia/métodos , Hemangioma Cavernoso/diagnóstico , Neoplasias das Glândulas Suprarrenais/cirurgia , Idoso , Diagnóstico Diferencial , Hemangioma Cavernoso/cirurgia , Humanos , Achados Incidentais , Neoplasias Pulmonares/diagnóstico por imagem , Imagem por Ressonância Magnética , Masculino , Doenças Raras/diagnóstico , Tomografia Computadorizada por Raios X
19.
J Clin Neurosci ; 58: 218-221, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30340970

RESUMO

Dural cavernous angiomas (CAs) outside the middle cranial fossa are uncommon vascular lesions that generally present with benign clinical course compared to those within the middle cranial fossa. Aggressive invasion of these lesions is less common and mainly involves the skull. Dura sinus invasion and diffused nodular growth are exceedingly rare. We presented a case of a 33-year-old male with multiple nodular CAs growing in a sheet-like pattern along the falx cerebri and convexity dura, which occluded the superior sagittal sinus, destructed calvarium and were associated with an isolated skull CA on the right forehead. Both dura sinus and convexity skull were extensively invaded by these multiple dural CAs without obvious mass effect, suggesting an aggressive infiltration pattern. Invasive dural CAs have been predominantly observed in patients <40 year-old and might be along the extra-axial vasculature. Therefore, cavernous angiomas should be considered in the diagnosis of dura-based invasive lesions and a closer follow-up might be recommended for young patients with dural CAs adjacent to dura sinus or skull.


Assuntos
Dura-Máter/patologia , Hemangioma Cavernoso/patologia , Adulto , Hemangioma Cavernoso/diagnóstico , Humanos , Masculino , Crânio/patologia , Seio Sagital Superior/patologia
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