Abstract:We report on two cases of hepatocellular carcinoma (HCC) with metastasis to the cavernous sinus and sphenoid sinus. Both cases presented with diplopia and retro-orbital headache and both underwent surgery for a primary pituitary gland tumor. After surgery, both cases were diagnosed with metastases from HCC. Case 1 was a 67-year-old male with a history of HCC who was referred to our hospital for pituitary tumor surgery. The tumor appeared to be in the sella turcica and to invade the sphenoid sinus and right cav… Show more
“…This occurred due to invasion of both cavernous sinuses and compression of cranial nerves III, IV and VI bilaterally, the extent of which has not been previously reported. 9–12 16 Moreover, the tumour had also invaded the clivus and sphenoid sinus. Similar clivus involvement has been reported before with HCC but not together with ophthalmoplegia and panhypopituitarism.…”
Pituitary metastases, especially from a primary hepatocellular carcinoma (HCC), are rare. Review of the literature revealed only few cases reporting pituitary metastases complicated by panhypopituitarism from HCC. Calvarial metastases from HCC are even more rare. Here, we present a unique case of primary HCC with metastases to both the calvarium and the pituitary causing panhypopituitarism and bilateral ophthalmoplegia, respectively. To our knowledge, this is the first reported case of two unique and rare complications from metastatic HCC.
“…This occurred due to invasion of both cavernous sinuses and compression of cranial nerves III, IV and VI bilaterally, the extent of which has not been previously reported. 9–12 16 Moreover, the tumour had also invaded the clivus and sphenoid sinus. Similar clivus involvement has been reported before with HCC but not together with ophthalmoplegia and panhypopituitarism.…”
Pituitary metastases, especially from a primary hepatocellular carcinoma (HCC), are rare. Review of the literature revealed only few cases reporting pituitary metastases complicated by panhypopituitarism from HCC. Calvarial metastases from HCC are even more rare. Here, we present a unique case of primary HCC with metastases to both the calvarium and the pituitary causing panhypopituitarism and bilateral ophthalmoplegia, respectively. To our knowledge, this is the first reported case of two unique and rare complications from metastatic HCC.
“…24 Second, since data on treatment of cases with brain metastases unavailable in the SEER database no further analysis is possible. The role of systemic treatment is not clear since only case reports on chemotherapy have been published to date 25 . Effects of sorafenib on brain metastases in HCC patients are not independently reported so far.…”
Background: There is little population-based data on hepatocellular carcinoma (HCC) with brain metastases at initial diagnosis published. This study aimed to estimate incidence of brain metastases in initial metastatic HCC and its impact on prognosis.
Methods: Newly diagnosed HCC cases from 2010 to 2015 in the Surveillance, Epidemiology, and End Results (SEER) database were screened for the presence of brain metastases. Data were stratified by age and ethnicity. Multivariable logistic and Cox regression were used to identify factors associated with brain metastases and factors associated with overall survival (OS) and cancer-specific survival (CSS), respectively. Kaplan-Meier method and log-rank test were used for survival analysis.
Results : 141 cases presenting with brain metastases were identified, accounting for 0.35% of all HCC cases and 2.37% of cases with metastatic HCC disease. The incidence rate was highest among cases with age 50-59 (2.74%), respectively. Ethnicity was not associated with the presence of brain metastases at the time of HCC diagnosis. However, African American patients presented significantly lower disease-specific survival (median time: 1month; interquartile range (IQR):0-3.0 months). Initial lung or bone metastasis was independently associated with an increased risk of the presence of brain metastases (odds ratio (OR) 12.62, 95%CI 8.40-18.97), but not associated with worse OS and CSS among brain metastases cases.
Conclusions: The study shows population-based incidence and survival of brain metastases at diagnosis of HCC. Brain metastases are most prevalent in initial metastatic HCC patients with lung or bone metastasis. The results may contribute to consider screening of the brain among HCC with initial lung or bone metastasis.
“…This was later confirmed by a blood test. On the other hand, the most common symptom of pituitary metastasis is DI [ 6 – 8 , 15 ], because the posterior lobe receives direct blood flow from systemic circulation [ 9 , 15 ]. However, Peppa et al described that the symptoms of metastasis to the pituitary gland are not specific and include fatigue, weight loss, dizziness, nausea, and vomiting.…”
Section: Discussionmentioning
confidence: 99%
“…Distinguishing metastasis to the pituitary gland from metastasis to the skull base (sphenoid sinus, cavernous sinus, and sella turcica) is very difficult because of the close proximity of these regions [ 15 ]. To establish a diagnosis, pathological confirmation is required.…”
Section: Discussionmentioning
confidence: 99%
“…For the treatment of metastatic pituitary tumors, Morita et al reported that there were no significant differences in survival times between surgical and nonsurgical treatments [ 9 ]. The vascularity of metastatic tumors is extremely rich; therefore, surgery is sometimes performed not only for palliation, but also for prevention of hemorrhage [ 15 ]. Additionally, surgery improves the quality of life and provides pathologic confirmation of the disease [ 11 ].…”
BackgroundMetastasis to the pituitary gland is extremely rare and is often detected incidentally by symptoms associated with endocrine dysfunction. Breast and lung cancer are the most common primary metastasizing to pituitary gland. Metastasis from hepatocellular carcinoma to the pituitary gland is extremely rare, with only 10 cases having been previously reported. We present here the first case of pituitary metastasis of hepatocellular carcinoma presenting with panhypopituitarism diagnosed by magnetic resonance imaging.Case presentationWe report the case of an 80-year-old Japanese woman who presented with the sudden onset of hypotension and bradycardia after having previously been diagnosed with hepatocellular carcinoma. Based on low levels of pituitary hormones, she was diagnosed with panhypopituitarism caused by metastasis of the hepatocellular carcinoma to the pituitary gland. Magnetic resonance imaging with arterial spin-labeling was effective in the differential diagnosis of the intrasellar tumor. The patient died despite hormone replacement therapy because of hypovolemic shock.ConclusionMetastasis to the pituitary gland causes various non-specific symptoms, so it is difficult to diagnose. The present case emphasizes the importance of diagnostic imaging in identifying these metastases. Clinicians should consider the possibility of pituitary metastasis in patients with malignant tumors who demonstrate hypopituitarism.
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