Pituitary Apoplexy in Pregnancy: What do We Know?

Abstract

Pituitary apoplexy refers to a rare clinical syndrome consisting of signs and symptoms that occur due to rapid expansion of the contents of the sella turcica. It can occur spontaneously or associated with pituitary tumors. It can have a broad clinical spectrum, but usually presents with severe headache, visual impairment and hypopituitarism. Sudden onset of symptoms associated to imagiologic confirmation makes the diagnosis. Surgical treatment is advised when there is important compression of the optic tract. We present a case report and a review of the literature on pituitary apoplexy in pregnancy. The cases were reviewed to obtain information on maternal characteristics, clinical presentation, diagnostic studies, therapeutic modalities and maternal and fetal outcomes. Our review found 36 cases of pituitary apoplexy in pregnancy. Most of the cases occurred in the second trimester of pregnancy and headache was the most frequent symptom at presentation. Surgical therapy was required in more than half of the patients. In what respect maternal and fetal outcomes, there were 3 cases of preterm delivery and one case of maternal death. Our clinical case and literature review reinforces the importance of an early diagnosis to avoid potential adverse consequences.

Keywords

pituitary apoplexy - endocrinology in pregnancy

Introduction

Pituitary apoplexy refers to a rare clinical syndrome consisting of signs and symptoms that occur due to rapid expansion of the contents of the sella turcica, due to hemorrhagic or ischemic events. It can occur spontaneously or associated with pituitary tumors. In many cases, pituitary apoplexy is the initial presentation of an adenoma. The etiology is multifactorial, but several precipitating factors have been described, including pregnancy.[1] [2] [3] [4] [5] [6] [7]

The clinical spectrum goes from asymptomatic or mild symptoms to a life-threatening situation, to both the mother and the fetus, particularly when associated with corticotropin deficiency and adrenal insufficiency. The diagnosis is made through the identification of the clinical syndrome associated with sella turcica imaging. Magnetic resonance imaging (MRI) is the most sensitive method to confirm the diagnosis by revealing a pituitary tumor with hemorrhagic and/or necrotic components.[4] [6]

The treatment of choice is conservative, but surgery might be required when there are important visual disturbances due to optic tract compression.[4] [7]

These study aims to report a case of a woman presenting with pituitary apoplexy during pregnancy who was treated with conservative management and also to present a review of the literature on this subject.

Methods

We report a case of pituitary apoplexy during pregnancy and present a review of the published cases in the literature on this subject. To identify these cases, we performed a research using PubMed/MEDLINE, using the MeSH terms ‘‘pituitary apoplexy” and ‘‘pregnancy.” We included all studies published until January 2021. Our search was limited to studies published as full-text articles in English or in Portuguese. All the articles without pituitary imaging were excluded. Written informed consent was obtained from the patient described in our case report. The selected cases were reviewed to obtain information on maternal characteristics, clinical presentation, diagnostic studies, therapeutic modalities and maternal and fetal outcomes. The collected data was analyzed and summarized in a table along with the author's name and respective reference ([Chart 1]).[1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] [30] [31] [32] [33] [34] [35] [36] [37]

Chart 1 Summary of available literature on pituitary apoplexy during pregnancy

Author [reference]	Age  (years)	Clinical presentation	GA	Pituitary imaging (MRI or CT)	Treatment (GA)	Evolution	Delivery
Prior lesion: Prolactinoma
Tandon et al.[37]	27	Headache, Visual defects	36WG	MRI: suprasellar, hemorrhagic mass with optic chiasm compression	Endoscopic endonasal transsphenoidal resection (36WG)	Resolution	C-section at term
Castro et al.[26]  -Case 2	32	Headache, nausea vomiting	28WG	MRI: intrapituitary hemorrhage	Steroids	Improvement	C-section at term
Prior lesion: Macroprolactinoma
Freeman et al.[8]	22	Headaches, diaphoresis, Visual defects, DI	32WG	MRI: pituitary hemorrhage, with optic chiasm compression and without neurohypophysis visualization	BCP stopped when pregnancy was diagnosed Transsphenoidal evacuation	Resolution	Delivery at term
Parihar et al.[34]	22	Headache, vomiting, vision loss	20WG	Pituitary apoplexy and compression over optic nerve and chiasm	BCP stopped when pregnancy was diagnosed  Transsphenoidal decompression, removal of hematoma	Resolution	Delivery at term
Grand'Maison S et al.[15]  -Case 2	30	Headache	20WG	MRI: pituitary mass with acute bleeding	Continued CBG (initiated before pregnancy)	Resolution	Vaginal delivery at term
Jemel M et al.[20]  -Case 2	35	Severe headache, nausea, vomiting deterioration of the visual field	22WG	MRI: a pituitary mass of compatible with a pituitary adenoma in apoplexy	CBG initiated before pregnancy Microsurgical transsphenoidal		Delivery at term
Oguz et al.[31]	26	Headache, nausea, visual defects, left  temporal deficit	22WG	MRI: macroadenoma with hemorrhage and optic chiasm compression	CBG  Transsphenoidal surgery	Improvement	C-section at term
Witek et al.[38]	25	Headaches, dizziness, Visual defects	14WG	MRI: tumor enlargement with optic chiasm displacement and focal hemorrhage	BCP stopped when pregnancy was diagnosed  Restarted BCP  Transsphenoidal adenomectomy (20WG)	Improvement	C-section at term
Gondim et al.[13]	29	Headache, visual defects	30WG	MRI: Macroadenoma with inside hemorrhage	Continued BCP (initiated before pregnancy)  Mini-invasive pituitary surgery (32WG)		Delivery at term
Janssen et al.[19]	27	Headache, visual defects	10WG	MRI: tumor growth, suprasellar extension and optic chiasm compression. Liquefaction within the tumor, indicating apoplexy	BCP stopped when pregnancy was diagnosed  Restarted BCP	Resolution	Vaginal delivery at term
Hayes et al.[17]	41	Visual defects	18WG	MRI: pituitary hemorrhage with a significant  increase in the size of the tumor	CBG stopped when pregnancy was diagnosed  Stereotactic endoscopic transsphenoidal excision (2nd trimester)		Vaginal delivery at term
Couture et al.[6]	37	Headache, Nausea, Visual defects	16WG	MRI: sellar mass with suprasellar extension and contact with the optic chiasm, compatible with hemorrhage in a pituitary  tumor	BCP switched to CBG when pregnancy was diagnosed	Resolution	C-section at term
Prior lesion: GHoma
Lunardi et al.[24]	21	Headache, Visual defects	24WG	CT: intrasellar space-occupying lesion with a marked suprasellar extension.	Transsphenoidal approach	Resolution; DI development	Normal delivery at term
Atmaca et al.[3]	33	Headache, Visual defects	33WG	MRI: Pituitary apoplexy	Transsphenoidal resection during labor		C-section at term
Prior lesion: ACTHoma (Nelson syndrome)
Gheorghiu et  al.[12]	33	Headache, nausea	22WG	MRI: intrasellar mass suggesting pituitary  apoplexy		DI development	Delivery at term
Prior lesion: Adenoma
Ohtsubo et al.[32]	29	Headache, vomiting,  Visual defects	24WG	CT and MRI: pituitary adenoma with  hematoma	Transsphenoidal approach  (32WG)		Delivery at term
Prior lesion: Macroadenoma
Iuliano et al.[18]	28	Headache, edema of the right optic disk	29WG	MRI: pituitary macroadenoma with hemorrhage and compression of the right optic nerve	BCP  Transnasal approach (29WG)	Resolution	Delivery at term
Unknown prior lesion
Murao et al. [30]	35	Nausea, vomiting	39WG	MRI: pituitary apoplexy
Kita et al.[21]	26	Visual defects	26WG	MRI: pituitary mass with a fluid level component displacing the optic chiasm	Endonasal  endoscopic surgery (27WG)	Improvement; DI development	Delivery at term
Krull et al.[2]	28	Headache, DI	7WG	MRI: pituitary apoplexy
Piantanida et al.[35]	27	Headache, Visual defects	35WG	MRI: sellar mass with suprasellar extension, with optic chiasm compression, deviation of the pituitary stalk, and with recent bleeding	Endonasal endoscopic transsphenoidal surgery. (postpartum)	Resolution	C-section at 35WG
Fujimaki et al.[9]	23	Headache, Visual defects	24WG	MRI: large mass occupying the pituitary fossa and suprasellar cistern	Surgery was performed 1 month postpartum	Improvement	C-section at 34WG
De Heide et al.[7]	26	Headache nausea, vomiting, Visual  defects, DI	23WG	MRI: pituitary tumor with hemorrhage		Improvement	Delivery at term
Bamfo et al.[4]	31	Vomiting, Visual defects, Unilateral ptosis	10WG	Hemorrhage into a preexisting solid or cystic lesion, with extension into the left cavernous sinus and optic chiasm compression			C-section at term
Lee et al.[23]	26	Headache, visual defects, low TSH and FSH and high T4, prolactin and somatomedin C	24WG	MRI: mass arising from the pituitary fossa and extending into the suprasellar cistern compressing the optic chiasm	Transsphenoidal surgery	Resolution	Vaginal delivery at term
Grand'Maison S et al.[15]  -Case 1	33	Headache, Visual defects, dizziness, neck stiffness	39WG	MRI/CT: sellar central hemorrhagic infarction and pituitary hyperplasia in contact with the optic chiasm			Labor induction at term
Abraham RR et al.[1]	32	Visual Defects decreased right V1-V2  facial	23WG	MRI: enlargement of the pituitary with hemorrhage and optic nerve compression	Emergent endoscopic endonasal surgery (23WG)
Jemel M et al.[20]  -Case 1	32	Headache, Visual defects	37WG	MRI: sellar central hemorrhagic infarction and pituitary hyperplasia, compatible with sub- acute pituitary apoplexy	None		Labor induction at term
Jemel M et al.[20]  -Case 3	30	Headache, Visual defects	24WG	MRI: bleeding within a macroadenoma	Endoscopic transsphenoidal ressection (24WG)	Improvement	Delivery at term
Castro et al.[26]  -Case 1	27	Headache, Visual defects	24WG	MRI: pituitary hemorrhage, with optic tract compression	Transsphenoidal partial excision of pituitary gland	Resolution; DI development	C-section at term
Mathur et al.[25]	34	Headache, neurological deficits, reversible vasoconstriction syndrome and stroke	Puer- perium	MRI: Pituitary apoplexy was diagnosed based on a pituitary hemorrhage	Steroids  Nimodipine plus lamotrigine for seizure prophylaxis	Resolution	Emergent c- section
Okafor et al.[33]	30	Headache, vomiting. protrusion of the right eye	24WG	CT scan: pituitary tumor with pressure effects, occluding the anterior horn of the left lateral ventricle. The other ventricles were dilated	BCP	Hypertension with encephalopathy, cardiac arrest and death	Emergent C- section at 34 + 5WG
Chan et al.[5]	28	Headache, Visual defect, hypogonadism, low TSH and high serum  prolactin	38WG	MRI: pituitary tumor, with hemorrhage and hypophysis and optic chiasm compression	Steroids  Transsphenoidal surgery 2 days after delivery	Improvement	Forceps at term
Galvão et al.[10]  - Case 1	30	Consciousness loss, Headache, Visual  defects	28WG	MRI: macroprolactinoma, with sellar and suprasellar hemorrhage	None	Resolution	C-section at term
Galvão et al.[10]  -Case 2	25	Headache, Visual defects		MRI: pituitary apoplexy	Transsphenoidal adenomectomy (2nd trimester)	Development of Hypothyroidism and DI	C-section at term
Cokmez et al.[16]	26	Headache, vomiting, Visual defects	24 WG	MRI: macroadenoma and bleeding	Steroids  Tumor excision was performed  with craniotomy	Improvement	C-section at term

Abbreviations: BCP, Bromocriptine; CBG, Cabergoline; CT, computed tomography; DI, Diabetes insipidus; GA, Gestational age; MRI, Magnetic resonance imaging; WG, weeks of gestation.

Case Report

A 36-year-old women, 30 weeks pregnant was admitted to the emergency service with severe holocranial headache, blurred vision, photophobia and vomiting for the last 4 days. In the day before she had been discharged from another hospital with the diagnosis of migraine. She had type 1 Diabetes Mellitus for 18 years, without known micro or macrovascular complications. She was on insulin (detemir and lispro), acetylsalicylic acid, folic acid, ferrous sulfate and potassium iodine. At admission, physical examination, blood pressure and neurologic examination were normal. Hemoglobin, platelets, renal and hepatic function were in the normal range and sFLT-1 /PLGF ratio was negative (<38), excluding pre-eclampsia as the cause of this clinical picture. Brain MRI was suggestive of pituitary apoplexy with compression and swelling of the optic tract: “Enlarged pituitary gland 12 mm in height, with heterogeneous sign. There is an evident suprasellar extension and shaping of the optic chiasm.” ([Fig. 1]) After neuro-ophthalmological examination, optic chiasm compression was excluded and surgery was postponed. Blood levels of ACTH, FT4, TSH and cortisol were unremarkable. She was started on intravenous hydrocortisone 100 mg every 8 hours, with progressive improvement of symptoms. At 35 weeks of gestation, an urgent c-section was performed because of a non-reassuring fetal heart rate tracing ([Fig. 1]) associated with absence fetal movements. A baby girl was born with 4080 g and an apgar index of 7/9. She was asymptomatic on discharge ([Fig. 2]). In the post-partum period she remained clinically stable, asymptomatic and she was diagnosed with a non-functioning macroadenoma. She suspended corticotherapy without relapse.

Fig. 1 MRI showing pituitary apoplexy and arrows indicating the pituitary gland.

Fig. 2 Non-reassuring fetal heart rate tracing on CTG.

Discussion

Pituitary apoplexy is a rare event and far less frequent in pregnancy. In the absence of more robust studies, the experience provided by case reports establishes an important guidance for managing these patients. The estimated prevalence of pituitary apoplexy is 1:10000 pregnancies at term, with a mean gestational age of diagnose of 24 weeks’ gestation and 10% of cases occurring in puerperium. In many cases, as in our case report, it constitutes the first presentation of a pituitary tumor, especially macroadenomas as they tend to be more hemorrhagic.[3] [14] [15]

Pituitary apoplexy can occur spontaneously or associated with pituitary tumors. The etiology is multifactorial, but several precipitating factors have been described: pregnancy (as in our clinical case), hemorrhagic disturbances, anticoagulation therapy, hypertension, diabetes mellitus, radiation or head trauma, cerebral aneurysm, major surgery, especially coronary artery bypass grafting, estrogen therapy, lumbar punction, upper respiratory tract infection, endocrine stimulation tests, initiation, or withdrawal of dopaminergic therapy.[1] [4] [5] [6] [7]

The typical presentation of pituitary apoplexy is the one described in our case, with sudden onset of severe bilateral headache, visual disturbances, nausea and vomiting and secondary symptoms to the involvement of cranial nerves (the oculomotor is the most frequently affected). The absence of classic symptoms can delay the diagnosis. In ∼80% of the cases, patients will develop deficiency of one or more anterior pituitary hormones, depending on the percentage of pituitary tissue destroyed. Gonadotrophins are the most affected, followed by ACTH and TSH and less frequently prolactin. In this case, gonadotrophins are difficult to value since they are physiologically braked in pregnancy.[1] [2] [3] [4]

Acute secondary adrenal insufficiency is seen in approximately two-thirds of patients with pituitary tumor apoplexy and it's the major source of mortality associated with the condition, requiring prompt corticosteroid replacement in anticipation.

The diagnosis is done in the presence of the clinical syndrome associated with sella turcica imaging. Magnetic resonance (MRI) is the most sensitive method to confirm the diagnosis and usually reveals a pituitary tumor with hemorrhagic and/or necrotic components.[4] [6]

In the pregnancy context the treatment of choice is conservative. Medical therapy includes corticotherapy, dopamine agonists, such as cabergoline and bromocriptine and reposition of hormonal deficits. Surgery might be required during pregnancy, when there are important visual disturbances due to compression, endocrinal hypersecretion (especially Cushing disease) or for life-threatening apoplexy.[4] [7] [14]

As a result of a literature research on Pubmed we found 36 case reports. From their analysis, we found that the average age of the pregnant women was 29 years old (±4 years), with an average gestational age of 25 weeks (±8 weeks) at diagnose. Most cases occurred in the second trimester. Regarding previously diagnosed lesions, it was present in 47% of patients. There were 7 cases of macroadenomas, 4 cases of microadenomas and 6 cases of adenomas without size specification. Therefore, pituitary apoplexy during pregnancy can be the first manifestation of an unrecognized pituitary adenoma in a large portion of this series. Headache was the most frequent symptom, being present in 86% of cases. Corticotherapy was used in 11% of cases and surgery was required in 61%. Most deliveries were uneventful. C-section was the mode of delivery in 15 cases, there were 6 cases of vaginal delivery and the route of delivery was unknown in 48% of the cases. There were 3 cases of preterm delivery and 28 term deliveries. There was one case of maternal death.

Conclusion

We consider our case report an example of successful management with conservative therapy, since our patient had sustained remission of symptoms without surgery and has already suspended medical treatment without relapse. We would like to reinforce that a precocious diagnosis is essential to a timely approach, avoiding the morbimortality potentially related to this condition.

Conflicts to Interest

The authos have no conflicts of interest to declare.

• References

• 1 Abraham RR, Pollitzer RE, Gokden M, Goulden PA. Spontaneous pituitary apoplexy during the second trimester of pregnancy, with sensory loss. BMJ Case Rep 2016; 2016: bcr2015212405
• 2 Al-Sharafi BA, Nassar OH. Successful pregnancy in a female with a large prolactinoma after pituitary tumor apoplexy. Case Rep Obstet Gynecol 2013; 2013: 817603
• 3 Atmaca A, Dagdelen S, Erbas T. Follow-up of pregnancy in acromegalic women: different presentations and outcomes. Exp Clin Endocrinol Diabetes 2006; 114 (03) 135-139
• 4 Bamfo JE, Sharif S, Donnelly T, Cohen MA, Golara M. A case of pituitary apoplexy masquerading as hyperemesis gravidarum. J Obstet Gynaecol 2011; 31 (07) 662
• 5 Chan JL, Gregory KD, Smithson SS, Naqvi M, Mamelak AN. Pituitary apoplexy associated with acute COVID-19 infection and pregnancy. Pituitary 2020; 23 (06) 716-720
• 6 Couture N, Aris-Jilwan N, Serri O. Microprolactinoma apoplexy in pregnancy, Endocrine Practice Vol 18,. 2012
• 7 de Heide LJM, van Tol KM, Doorenbos B. Pituitary apoplexy presenting during pregnancy. Neth J Med 2004; 62 (10) 393-396
• 8 Freeman R, Wezenter B, Silverstein M. et al. Pregnancy-associated subacute hemorrhage into a prolactinoma resulting in diabetes insipidus. Fertil Steril 1992; 58 (02) 427-429
• 9 Fujimaki T, Hotta S, Mochizuki T. et al. Pituitary apoplexy as a consequence of lymphocytic adenohypophysitis in a pregnant woman: a case report. Neurol Res 2005; 27 (04) 399-402
• 10 Galvão A, Gonçalves D, Moreira M, Inocêncio G, Silva C, Braga J. Prolactinoma and pregnancy – a series of cases including pituitary apoplexy. J Obstet Gynaecol 2016
• 11 Garrão A. et al. Livro de Endocrinologia e Gravidez. Grupo Estudos Endocrinol Gravidez 2018
• 12 Gheorghiu ML, Chirita C, Coculescu M. Partial remission of Nelson's syndrome after pituitary apoplexy during pregnancy. Endocrin Abstr 2009; 19: 191
• 13 Gondim J, Ramos Júnior F, Pinheiro I, Schops M, Tella Júnior OI. Minimally invasive pituitary surgery in a hemorrhagic necrosis of adenoma during pregnancy. Minim Invasive Neurosurg 2003; 46 (03) 173-176
• 14 Graillon, et al. Surgical indications for pituitary tumors during pregnancy: a literature review. Pituitary 2019
• 15 Grand'Maison S, Weber F, Bédard MJ, Mahone M, Godbout A. Pituitary apoplexy in pregnancy: A case series and literature review. Obstet Med 2015; 8 (04) 177-183
• 16 Cokmez H, Bayram C. Pituitary apoplexy developing during pregnancy: escape from the verge of death,. Clinical and Experiment Obstetrics and Gynecology, 2020
• 17 Hayes AR, O'Sullivan AJ, Davies MA. Endocrinol Diabetes Metab Case Rep 2014
• 18 Iuliano S, Laws Jr ER. Management of pituitary tumors in pregnancy. Semin Neurol 2011; 31 (04) 423-428
• 19 Janssen NM, Dreyer K, van der Weiden RM. Management of pituitary tumour apoplexy with bromocriptine in pregnancy. JRSM Short Rep 2012; 3 (06) 43
• 20 Jemel M, Kandara H, Riahi M, Gharbi R, Nagi S, Kamoun I. Gestational pituitary apoplexy: Case series and review of the literature. J Gynecol Obstet Hum Reprod 2019; 48 (10) 873-881
• 21 Kita D, Hayashi Y, Sano H. et al. Postoperative diabetes insipidus associated with pituitary apoplexy during pregnancy. Neuroendocrinol Lett 2012; 33 (02) 107-112
• 22 Krull I, Christ E, Kamm CP, Ganter C, Sahli R. Hyponatremia associated coma due to pituitary apoplexy in early pregnancy: a case report. Gynecol Endocrinol 2010; 26 (03) 197-200
• 23 Lee MS, Pless M. Apoplectic lymphocytic hypophysitis. Case report. J Neurosurg 2003; 98 (01) 183-185
• 24 Lunardi P, Rizzo A, Missori P, Fraioli B. Pituitary apoplexy in an acromegalic woman operated on during pregnancy by transphenoidal approach. Int J Gynaecol Obstet 1991; 34 (01) 71-74
• 25 Mathur D, Lim LF, Mathur M, Sng BL. Pituitary apoplexy with reversible cerebral vasoconstrictive syndrome after spinal anaesthesia for emergency caesarean section: an uncommon cause for postpartum headache. Anaesth Intensive Care 2014; 42 (01) 99-105
• 26 Melo Castro D, Mendes A, Pinto C, Gonçalves J, Braga J. Pituitary apoplexy during pregnancy – two cases reports. Acta Obstet Ginecol Port 2015; 9 (03) 267-270
• 27 Miranda M, Barros L, Knopfelmacher M. et al. [Pituitary apoplexy followed by endocrine remission. Report of two cases]. Arq Neuropsiquiatr 1998; 56 (3A): 449-452
• 28 Molitch ME. Pituitary disorders during pregnancy. Endocrinol Metab Clin North Am 2006; 35 (01) 99-116 , vi
• 29 Molitch ME. Prolactinoma in pregnancy. Best Pract Res Clin Endocrinol Metab 2011; 25 (06) 885-896
• 30 Murao K, Imachi H, Muraoka T, Ishida T. Hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome with pituitary apoplexy. Fertil Steril 2011; 96 (01) 260-261
• 31 Oguz S. et al. A case of atypical macroprolactinoma presenting with pituitary apoplexy during pregnancy and review of the literature. Gynecol Endocrinol 2019
• 32 Ohtsubo T, Asakura T, Kadota K. et al. [A report of a transsphenoidal operation during pregnancy for a pituitary adenoma]. No Shinkei Geka 1991; 19 (09) 867-870
• 33 Okafor UV, Onwuekwe IO, Ezegwui HU. Management of pituitary adenoma with mass effect in pregnancy: a case report. Cases J 2009; 2: 911
• 34 Parihar V, Yadav YR, Sharma D. Pituitary apoplexy in a pregnant woman. Ann Indian Acad Neurol 2009; 12 (01) 54-55
• 35 Piantanida E, Gallo D, Lombardi V. et al. Pituitary apoplexy during pregnancy: a rare, but dangerous headache. J Endocrinol Invest 2014; 37 (09) 789-797
• 36 Scherrer H, Turpin G, Darbois Y, Metzger J, de Gennes JL. [Pregnancy and hyperprolactinemia. Review of therapeutic measures apropos of a series of 35 patients]. Ann Med Interne (Paris) 1986; 137 (08) 621-626
• 37 Tandon A, Alzate J, LaSala P, Fried MP. Endoscopic endonasal transsphenoidal resection for pituitary apoplexy during the third trimester of pregnancy. Surg Res Pract 2014; 2014: 397131
• 38 Witek P, Zieliński G, Maksymowicz M, Zgliczyński W. Transsphenoidal surgery for a life-threatening prolactinoma apoplexy during pregnancy. Neuroendocrinol Lett 2012; 33 (05) 483-488
• 39 Zhang R. et al. Complex effects of apoplexy secondary to pituitary adenoma. Rev Neurosci 2016

Publikationsverlauf

Eingereicht: 05. Februar 2022

Angenommen: 21. März 2023

Artikel online veröffentlicht:
20. Juni 2023