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. 2010 Nov 2;1(4):187–196. doi: 10.1007/s12672-010-0041-7

Table 1.

Clinical manifestation of patients with craniopharyngioma at the diagnosis

Patients Sex Age at the diagnosis (years) Endocrine involvement Hypothalamic dysfunctions Neurological manifestations Visual disturbances
1 M 6 Hyperprolactinemia Somnolence Headache Diplopia
2 M 6 GHD OB Headache, nausea/vomit Visual deterioration
3 F 7 GHD Weight loss Headache, nausea/vomit TQ RE
4 F 15 GHD, HG, HC Somnolence Headache, nausea/vomit Papilloedema, optic atrophy LE, BH
5 F 8 No Hyperphagia, OB, somnolence Headache, hemiparesis, ptosis LE AM
6 M 9 GHD, HC, hyperprolactinemia Somnolence Headache, nausea/vomit AM LE/TH RE
7 F 10 DI OB Headache Papilloedema, TH LE
8 M 14 No OB Headache BH
9 M 16 GHD, DI, HT, HG, HC
10 M 20 No OB BH
11 F 21 DI, HT, HG, HC, hyperprolactinemia Headache, nausea/vomit BH
12 F 22 GHD, HT, HG, HC OB Headache BH
13 M 26 GHD, DI, HT, HG, HC OB
14 F 27 DI, HG, HC Somnolence Nausea/vomit
15 M 30 HT, HG, HC Hyperphagia, OB, somnolence Headache Diplopia
16 F 55 No Weight loss TQ LE

M male, F female, DI diabetes insipidus, GHD growth hormone deficiency, HT hypothyroidism, HG hypogonadism, HC hypocortisolism, OB obesity, LE left eye, RE right eye, BH bitemporal hemianopsia, AM amaurosis, TH temporal hemianopsia, TQ temporal quadranopsia