DESPITE THEIR UNIQUE clinical, radiological, and surgical consideratio
ns, diaphragma sellae meningiomas remain largely undistinguished from
tuberculum sellae meningiomas. On the basis of our experience with 12
patients with diaphragma sellae meningiomas and our review of the lite
rature, we classify these tumors into three groups: Type A, originatin
g from the upper leaf of the diaphragma sellae anterior to the pituita
ry stalk; Type B, originating from the upper leaf of the diaphragma se
llae posterior to the pituitary stalk; and Type C, originating from th
e inferior leaf of the diaphragma sellae. Each type has specific clini
cal symptoms. Type A mainly presents with unilateral visual disturbanc
es and visual field defects resembling those of tuberculum sellae meni
ngiomas, although preoperative diabetes insipidus occurred in patients
with large tumors. Type B causes fewer visual disturbances, but memor
y disturbance and hypopituitarism occur. Type C closely resembles nonf
unctioning pituitary adenomas; bitemporal hemianopsia and hypopituitar
ism are common. Multiplanar magnetic resonance images can accurately d
iagnose the tumor and establish its type. Surgical approaches include
the cranio-orbital approach for Types A and B and the transcranial-tra
nssphenoidal approach for Type C. Surgery is more difficult than for t
uberculum sellae meningiomas because of the deep location and the diff
iculty of dissecting Types A and B from the pituitary stalk. Repair of
the sphenoid sinus to prevent cerebrospinal fluid leakage is mandator
y for Type C tumors.