Primary Tumour Type, Clinical Features, Treatment and Outcome of Patients with Iris Metastasis

Author(s):  
Tao Liu ◽  
Feng Bai ◽  
Li Yang ◽  
Li Liu ◽  
Jun Xiao ◽  
...  
2015 ◽  
Vol 41 (2) ◽  
pp. e41-e55 ◽  
Author(s):  
Anna S. Berghoff ◽  
Aysegül Ilhan-Mutlu ◽  
Carina Dinhof ◽  
Manuel Magerle ◽  
Monika Hackl ◽  
...  

Pituitary ◽  
2021 ◽  
Author(s):  
Alberto Ragni ◽  
Alice Nervo ◽  
Mauro Papotti ◽  
Nunzia Prencipe ◽  
Francesca Retta ◽  
...  

Abstract Purpose Pituitary metastases (PM) are uncommon findings and are mainly derived from breast and lung cancers. No extensive review of PM from neuroendocrine neoplasms (NENs) is on record. Here we describe a clinical case of PM from pancreatic NEN and review the clinical features of PM from NENs reported in the literature. Methods A case of PM from a pancreatic NEN followed at our institution is described. We also reviewed the 43 cases of PM from NENs reported in the literature. Results A 59-year old female patient, previously submitted to duodeno-cephalo-pancreasectomy for a well-differentiated pancreatic NEN, with known hepatic metastases, underwent a 68 Ga-DOTATOC PET/CT that revealed an uptake in the pituitary gland. A subsequent MRI displayed a pituitary lesion, with suprasellar extension. After a hormonal and genetic diagnostic workup that excluded the diagnosis of MEN 1, the worsening of headache and visual impairment and the growth of the lesion lead to its surgical removal. A pituitary localization of the pancreatic NEN was identified. Regarding the published cases of PM from NENs, the most common tumour type was small cell lung cancer (SCLC), accounting for nearly half of the cases, followed by bronchial and pancreatic well differentiated NENs. The most frequent symptom was a variable degree of visual impairment, while headache was reported in half of the cases. Partial or total anterior hypopituitarism was present in approximately three quarters of the cases, while diabetes insipidus was less common. The most frequent treatment for PM was surgical resection, followed by radiotherapy and chemotherapy. The clinical outcome was in line with previous reports of PM from solid tumours, with a median survival of 14 months. Surgery of PM was associated with prolonged survival. Conclusions PM from NENs have clinical features similar to metastases derived from other solid tumours, albeit the involvement of the anterior pituitary seems more frequent; a thorough pituitary hormonal evaluation is mandatory, after focused radiological studies, particularly if a surgical approach is considered. The optimal management of PM remains disputed and seems mainly driven by the aggressiveness of the primary tumour and the presence of symptoms. In well-differentiated NENs, particularly in the case of symptomatic PM, surgical removal may be a reasonable approach.


Author(s):  
Steven David Brass ◽  
Marie-Christine Guiot ◽  
Steffen Albrecht ◽  
Rafael Glikstein ◽  
Gérard Mohr

Objective:Hemangiopericytoma is an aggressive vascular tumour that rarely affects the central nervous system and is even more rarely spinal in presentation. The clinical features of a patient with a recurrent extraspinal hemangiopericytoma presenting with an epidural spinal cord compression by local invasion are described, including a review of the literature on metastatic hemangiopericytoma to the spine.Methods:A case of a 53-year-old male, with a recurrent extraspinal hemangiopericytoma which metastasized to the thoracic spine five years after detection of the primary tumour is presented. A chart review was conducted where all pertinent history, physical, laboratory, and radiological data were collected. A Pub-Med search using the keyword “hemangiopericytoma” identified all reported cases documenting clinical features, treatment, recurrence and outcome with respect to metastatic hemangiopericytoma to the spine.Results:Nine patients have been reported to have metastatic hemangiopericytoma to the spine. The median patient age was 47 years and there was a slight male preference. An unusual feature of the hemangiopericytoma is the prolonged period, up to 16 years, between the diagnosis of the primary hemangiopericytoma and the metastases to the spine. All patients were treated with a combination of radiation and surgery.Conclusion:Hemangiopericytomas show a slow clinical evolution with a strong propensity to relapse long after previous treatment and thus, once identified, prolonged follow-up for recurrence is indicated. A close follow-up of these patients is required because of frequent recurrences and delayed metastases even if the primary lesion was well-controlled. Although overall uncommon, hemangiopericytoma should be kept in mind in the differential diagnosis of vascular epidural spinal cord tumours.


2021 ◽  
Vol 8 (1) ◽  
pp. 21-XX
Author(s):  
Shalina Kaur ◽  
Noor Dina Hashim ◽  
Afiza Izura M Mohammad Sofi ◽  
Gurdev Singh Naraman Singh ◽  
Khairil Amir Sayuti

Pleomorphic adenoma provides as much as 40-70% of tumors in the minor salivary gland with the palate being the most frequent area engaged. Head and neck tumors in parapharyngeal space amount to less than 1%. We share a case of pleomorphic adenoma primarily arising in parapharyngeal space. This report highlights clinical features, pathology, radiological findings, and treatment of this tumor.


2001 ◽  
Vol 120 (5) ◽  
pp. A563-A564
Author(s):  
M ISMAIL ◽  
I DABOUL ◽  
B WATERS ◽  
J FLECKENSTEIN ◽  
S VERA ◽  
...  

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