Post operative pituitary apoplexy in a case of giant pituitary adenoma

T. Govindan, D. Sivashanmugam
{"title":"Post operative pituitary apoplexy in a case of giant pituitary adenoma","authors":"T. Govindan, D. Sivashanmugam","doi":"10.5580/44a","DOIUrl":null,"url":null,"abstract":"Giant pituitary adenomas are relatively rare and their management challenging. This article presents such a case, which developed post operative pituitary apoplexy. The case details and the pertinent literature are discussed. Introduction Giant pituitary adenomas are relatively rare tumors and their management complex and challenging . Most present with a combination of visual and endocrinological dysfunction . Surgical approach could be trans sphenoidal, trans cranial, or a combination of the two . While total excision has been reported, the occurrence of complications, especially pituitary apoplexy, and the generally poor prognosis following this are reported sporadically but well documented 2, 4, . This article presents one such case and reviews the literature. Case Report A 49 years old Tanzanian, was referred to our institution as a case of giant pituitary adenoma, which was diagnosed about a year back in Tanzania, where he had sought medical advice for visual problems. Examination revealed a well built, obese individual, with gynaecomasia, visual defects in the form of no PL in the left eye and 3/60 vision in the lower nasal quadrant of the right eye, and bilateral POA in both fundi. Plain x ray skull lateral showed a ballooned sella. Plain and contrast enhanced CT of the brain showed a large sellar, supra sellar and intra sphenoidal sinus mass, extending up to the level of the corpus callosum, with no hydrocephalus. MRI (plain and contrast enhanced) and MRA confirmed the same. His hormonal work-up was within normal limits. Pre operative contrast enhanced CT Pre operative contrast enhanced MRI He was adequately prepared with steroids and intra nasal antibiotics and taken up for a trans sphenoidal approach to the mass. The tumor was encountered in the sphenoidal sinus itself as expected. It was quite vascular and very fibrous, thus limiting the surgery to the sphenoidal and sellar portion of the tumor. He was kept sedated and ventilated post operatively; during the times he could be assessed when light on sedation, he was conscious with no focal neurological deficit. Biopsy was reported as typical of pituitary adenoma. About 14 hours post surgery, he suddenly developed hypotension, which required ianotrophs. Within half an hour, he became totally unconscious (GCS 3/15), with dilated and non reactive pupils. He soon developed features of frank diabetes insipidus, which was appropriately tackled. Plain CT scan brain, once he was stable to be shifted, showed intra tumoral bleed, enlarging the adenoma; there was also pan ventricular hemorrhage with hydrocephalus. Post operative plain CT Bilateral frontal EVDs were inserted, with no subsequent improvement. He was soon assessed to be brain dead and expired after 24 hours of the ictus. Discussion Pituitary adenomas whose size exceeds 4 cms are called giant pituitary adenomas . Giant pituitary adenomas are not special entities by themselves but unusual examples of locally invasive tumors 2 . These tumors present with higher frequency of ophthalmic and endocrinological dysfunctions, with poor results following surgical treatment . Initial surgical route is trans sphenoidal, followed by trans cranial, in case of lateral extension 3 or a combination of both. It is best to avoid aggressive surgery; partial resection followed by irradiation, combined with shunt procedure, if hydrocephalus is present, is ideal 1, . Post operative pituitary apoplexy carries a very poor prognosis 4 . This is characterized by worsening of vision, deterioration in conscious level and/or hormonal dysfunction. The possible reasons for the apoplexy are 1. the rapidly growing adenoma outstrips blood supply, leading to ischemic necrosis of the gland; 2. the large tumor itself may distort the infundibulum, thus compromising blood supply; leading to gland ischemia, with secondary bleeding; 3. the sudden release of perforating vessels from the internal carotids, after tumor debulking, can also lead to post operative bleeding; 4. The manipulation of the tumor during surgery can lead to post operative swelling and break through bleeding. Giant pituitary adenomas are difficult entities to treat and a less aggressive surgical approach seems an appropriate way to tackle these tumors. References 1. Symon L, Jakubowski J, Kendal B. Surgical treatment of giant pituitary adenomas. Journal of Neurology, Neurosurgery and Psychiatry1979; 42: 973 – 982. (s) 2. Garibi J, Pomposa I, Villar G, Gastambide S. Giant pituitary adenomas: clinical characteristics and surgical results. British Journal of Neurosurgery April 2002; 16, 2: 133 – 139 (7). (s) 3. Wesley A King, Gerald E Rodts Jr, Donald P Becker, Duncan Q Mc Bride. Microsurgical management of giant pituitary tumors – Skull base surgery 1996, January 6(1): 17 – 26. (s) 4. Ahmad Faiz U, Pandey Paritosh, Mahapatra Ashok K. Post operative pituitary apoplexy in giant pituitary adenomas: a series of cases. Neurology India 2005,53(3): 326 – 328. (s) 5. Atul Goel, Dattatriya Muzumdar, Surgical management of giant pituitary adenomas. International Congress Series (1259) 2004: 99 – 106. 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Abstract

Giant pituitary adenomas are relatively rare and their management challenging. This article presents such a case, which developed post operative pituitary apoplexy. The case details and the pertinent literature are discussed. Introduction Giant pituitary adenomas are relatively rare tumors and their management complex and challenging . Most present with a combination of visual and endocrinological dysfunction . Surgical approach could be trans sphenoidal, trans cranial, or a combination of the two . While total excision has been reported, the occurrence of complications, especially pituitary apoplexy, and the generally poor prognosis following this are reported sporadically but well documented 2, 4, . This article presents one such case and reviews the literature. Case Report A 49 years old Tanzanian, was referred to our institution as a case of giant pituitary adenoma, which was diagnosed about a year back in Tanzania, where he had sought medical advice for visual problems. Examination revealed a well built, obese individual, with gynaecomasia, visual defects in the form of no PL in the left eye and 3/60 vision in the lower nasal quadrant of the right eye, and bilateral POA in both fundi. Plain x ray skull lateral showed a ballooned sella. Plain and contrast enhanced CT of the brain showed a large sellar, supra sellar and intra sphenoidal sinus mass, extending up to the level of the corpus callosum, with no hydrocephalus. MRI (plain and contrast enhanced) and MRA confirmed the same. His hormonal work-up was within normal limits. Pre operative contrast enhanced CT Pre operative contrast enhanced MRI He was adequately prepared with steroids and intra nasal antibiotics and taken up for a trans sphenoidal approach to the mass. The tumor was encountered in the sphenoidal sinus itself as expected. It was quite vascular and very fibrous, thus limiting the surgery to the sphenoidal and sellar portion of the tumor. He was kept sedated and ventilated post operatively; during the times he could be assessed when light on sedation, he was conscious with no focal neurological deficit. Biopsy was reported as typical of pituitary adenoma. About 14 hours post surgery, he suddenly developed hypotension, which required ianotrophs. Within half an hour, he became totally unconscious (GCS 3/15), with dilated and non reactive pupils. He soon developed features of frank diabetes insipidus, which was appropriately tackled. Plain CT scan brain, once he was stable to be shifted, showed intra tumoral bleed, enlarging the adenoma; there was also pan ventricular hemorrhage with hydrocephalus. Post operative plain CT Bilateral frontal EVDs were inserted, with no subsequent improvement. He was soon assessed to be brain dead and expired after 24 hours of the ictus. Discussion Pituitary adenomas whose size exceeds 4 cms are called giant pituitary adenomas . Giant pituitary adenomas are not special entities by themselves but unusual examples of locally invasive tumors 2 . These tumors present with higher frequency of ophthalmic and endocrinological dysfunctions, with poor results following surgical treatment . Initial surgical route is trans sphenoidal, followed by trans cranial, in case of lateral extension 3 or a combination of both. It is best to avoid aggressive surgery; partial resection followed by irradiation, combined with shunt procedure, if hydrocephalus is present, is ideal 1, . Post operative pituitary apoplexy carries a very poor prognosis 4 . This is characterized by worsening of vision, deterioration in conscious level and/or hormonal dysfunction. The possible reasons for the apoplexy are 1. the rapidly growing adenoma outstrips blood supply, leading to ischemic necrosis of the gland; 2. the large tumor itself may distort the infundibulum, thus compromising blood supply; leading to gland ischemia, with secondary bleeding; 3. the sudden release of perforating vessels from the internal carotids, after tumor debulking, can also lead to post operative bleeding; 4. The manipulation of the tumor during surgery can lead to post operative swelling and break through bleeding. Giant pituitary adenomas are difficult entities to treat and a less aggressive surgical approach seems an appropriate way to tackle these tumors. References 1. Symon L, Jakubowski J, Kendal B. Surgical treatment of giant pituitary adenomas. Journal of Neurology, Neurosurgery and Psychiatry1979; 42: 973 – 982. (s) 2. Garibi J, Pomposa I, Villar G, Gastambide S. Giant pituitary adenomas: clinical characteristics and surgical results. British Journal of Neurosurgery April 2002; 16, 2: 133 – 139 (7). (s) 3. Wesley A King, Gerald E Rodts Jr, Donald P Becker, Duncan Q Mc Bride. Microsurgical management of giant pituitary tumors – Skull base surgery 1996, January 6(1): 17 – 26. (s) 4. Ahmad Faiz U, Pandey Paritosh, Mahapatra Ashok K. Post operative pituitary apoplexy in giant pituitary adenomas: a series of cases. Neurology India 2005,53(3): 326 – 328. (s) 5. Atul Goel, Dattatriya Muzumdar, Surgical management of giant pituitary adenomas. International Congress Series (1259) 2004: 99 – 106. (s) This article was last modified on Tue, 05 Jan 10 22:10:52 -0600
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巨大垂体腺瘤术后脑卒中1例
巨大垂体腺瘤相对罕见,其治疗具有挑战性。本文报告一例术后发展为垂体中风的病例。讨论了病例细节和相关文献。垂体巨大腺瘤是一种较为罕见的肿瘤,其治疗复杂且具有挑战性。多数表现为视觉和内分泌功能障碍。手术入路可经蝶骨、经颅或两者结合。虽然有完全切除的报道,但并发症的发生,特别是垂体中风,以及随之而来的普遍不良预后的报道虽然零星但文献记载充分2,4。本文提出了一个这样的病例,并回顾了文献。病例报告一名49岁的坦桑尼亚人,因巨大垂体腺瘤被转介到我们的机构,大约一年前,他在坦桑尼亚因视力问题寻求医疗建议而被诊断出来。检查显示:体格良好,肥胖,患有妇科疾病,左眼无PL,右眼下鼻腹3/60视力缺陷,双侧眼底POA。头颅侧位x线平片示蝶鞍膨大。颅脑CT平扫及增强显示大鞍、鞍上及蝶窦内肿块,延伸至胼胝体水平,未见脑积水。MRI(平扫增强)和MRA均证实相同。他的荷尔蒙检查结果在正常范围内。术前增强CT术前增强MRI他准备了充分的类固醇和鼻内抗生素,并采取了经蝶窦入路的肿块。不出所料,肿瘤发生在蝶窦内。它有很多血管和纤维,因此限制了手术在肿瘤的蝶骨和鞍部。术后保持镇静和通气;在这段时间里,他可以在服用镇静剂时进行评估,他是有意识的,没有局灶性神经缺陷。活检报告为典型的垂体腺瘤。手术后大约14小时,他突然出现低血压,需要抗营养品。半小时内,他完全失去知觉(GCS 3/15),瞳孔扩大且无反应。他很快就出现了尿崩症的特征,并得到了适当的治疗。颅脑CT平扫,待稳定移位后,显示瘤内出血,腺瘤增大;同时伴有脑积水的泛脑室出血。术后CT平片置入双侧额部evd,无后续改善。他很快被诊断为脑死亡,并在24小时后死亡。垂体腺瘤的大小超过4厘米称为巨大垂体腺瘤。巨大垂体腺瘤本身并不是一种特殊的实体,而是局部侵袭性肿瘤的罕见例子2。这些肿瘤表现为眼科和内分泌功能障碍的频率较高,手术治疗后效果较差。最初的手术路径是经蝶骨,其次是经颅,如果是侧伸3或两者结合。最好避免积极的手术;如果存在脑积水,理想的治疗方法是部分切除,然后放疗,再结合分流术。术后垂体卒中预后很差。其特点是视力恶化,意识水平下降和/或激素功能障碍。引起中风的可能原因有:1。快速生长的腺瘤超过血液供应,导致腺体缺血性坏死;2. 大肿瘤本身可能扭曲十二指肠,从而影响血液供应;导致腺体缺血,继发性出血;3.肿瘤缩小后,内颈动脉穿孔血管的突然释放也可导致术后出血;4. 手术过程中对肿瘤的操作可能导致术后肿胀和突破出血。巨大的垂体腺瘤是难以治疗的实体和一个较小的侵略性的手术方法似乎是一个适当的方式来解决这些肿瘤。引用1。张建军,张建军,张建军,等。垂体腺瘤的外科治疗。神经病学,神经外科和精神病学杂志1979;[42]: 973 - 982。(s) 2。李建军,李建军,李建军,等。垂体腺瘤的临床特征及手术效果。英国神经外科杂志2002年4月;(2).(2): 133 - 139(7)。韦斯利·A·金,杰拉德·E·罗兹,唐纳德·P·贝克尔,邓肯·Q·麦克布莱德。巨型垂体瘤的显微外科治疗-颅底外科1996,1月6日(1):17 - 26。(s) 4。Ahmad Faiz U, Pandey Paritosh, Mahapatra Ashok .巨大垂体腺瘤术后垂体卒中:一系列病例。中国神经病学杂志,2005,35(3):326 - 328。(s) 5。 Atul Goel, Dattatriya Muzumdar,巨大垂体腺瘤的外科治疗。国际会议系列(1259)2004:99 - 106。这篇文章最后一次修改是在1月5日星期二22:10:52 -0600
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