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Pictorial Essay
The Hippocampus: Normal Anatomy and Pathology
L AnneHayman1,
GregoryN.Fuller2,José
E.Cavazos3,
MarkJ. Pfleger4,
ChristinaA.Meyers5,EdwardF.Jackson6

T he hippocampi are unique and vital orly, it becomes the cingulate gyms; anteroinfe tenor tail. In humans, this gyms continues as
regions found in each of the cere riorly, it becomesthe paraterniinal gyms. The the vestigial supracallosalgyrus (indusium gri
bral hemispheres. In most subjects, smaller, inner limbic gyms contains the hip seum), and anteroinferiorly it is renamed the
the dominant left hippocampus primarily medi pocampus, which is subdivided into three seg vestigial paraterminalgyms.
ates verbal learning and memory, whereasthe ments: the bulbous anterior head (also called Anatomic coronal sections are traditionally
nondominant right side primarily mediates non the pesor foot), the body, and the slenderpos shownonly at the mid body ofthe hippocampus
verbal memory. Becausebilateral hippocampal
lesionsresult in amnesia(i.e., inability to learn
new information), extensive hippocampal re
search has been undertaken. The advent of sur @J).

gical procedures that can cure medically


intractableseizuresby excisionof hippocampal t frur@;)- .@“-.
abnormalities also has spurred extensive re
@ search directed toward MR analysis of this re Paraterminal
gyros - Parahippocampal
gyrue
gion. Our purpose is to introduce the reader to
these techniques. This paper is divided into @. , Vesti@ supracallosal
‘¿ .. - -. gyms (induseum griseum)
three parts: normal hippocampal anatomy, MR
@ imaging techniques,andrefractoryepilepsy. :. ,@ Tail

Normal Hippocampal Anatomy


The limbic lobe is formed by two gyri on the Vestigialparaterminalgyros Body
medial surface of each cerebral hemisphere. Head(foot,pes)
The larger outer gyms is renamed as it encircles
the corpus callosum (Fig. 1). Posteroinferiorly, Fig.1.—Limbic
lobeanatomy.
Drawings
showsubdivisions
ofouterandinner
it is calledthe parahippocampal gyrus;superi limbiclobegyri.

ReceivedJanuary22,1998;acceptedafterrevisionMarch10,1998.
1Department of Radiology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030-3498. Address correspondence to L A. Hayman.

2 Department of Neuropathology, University ofTexas M. D. Anderson Cancer Center, Houston, TX 77030.

3Departmentof Neurology,Universityof ColoradoHealthSciencesCenter,Denver,CO80262.


4Departmentof Radiology,OverlakeMedicalCenter,Bellevue,WA98004.
5 Department of Neuro-oncology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030.

tDepartmentof DiagnosticRadiology,UniversityofTexasM. D.AndersonCancerCenter,Houston,TX77030.


AJR1998;171:1
139—1
1460361—803X/98/1714—1
139©AmericanRoentgenRaySociety

AJR:171,October1998 1139
Hayman et al.

I
e
m
Temporal Horn
p
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. . .

C A
@ m . . ;. ... .. . @. (Fusiform

@ S
b J@.. @. @: . \gyrus

@
e
r
n
e
n
t
..
/1'
I COLLATERAL SULCUS

H
Residual cleft with cyst in 10-20% of normals
0

n
—¿
Dentate
gyrus
(molecular
cell
layer)
CA = CORNUAMMONS(Ammon's horn)(pyramidalcell layer)
—¿
CAl
@ —¿
CA2 CA4
(end
folium)
A B
Fig.2.—Hippocampal
anatomy.
A,Drawing ofaxialsection
oflefthippocampus
seenfrombelowshowsrotation
ofhippocampusanditsrelationship
withdentate
gyrus.
(Modifiedwithpermissionfrom11])
B,Drawingofcoronalsectionatmidbodyoflefthippocampus
showscross-sectional
relationship
betweenhippocampusandsurrounding
structures.
(Modifiedwithpermis
sionfrom [41)

(Fig. 2) 11—5].
At this level, it consistsof two in long axis of the temporal horn. However, even obliterated laterally in utero and may not be
terlocking laminae of gray matter: the cornu high-field-strength I .5-T MR imaging shows visualized (or only a small portion is visible).
ammonis (Ammon's horn) and the dentategy little of the cellular anatomy (Fig. 3). Rather, The hippocampal sulcus is found between the
flis. The comu ammonis can be divided into it defines the outline of the three major fis dentate gyrus and the subiculum and cornu
four microscopic zones of granular cells: sures: hippocampal, fimbriodentate, and chor ammonis. Small remnants of the hippocampal
CAl, CA2, CA3, and CA4 (Fig. 2). This oidal, which allows the reader to infer the sulcus (fissure) should not be mistaken as pa
coronal section simplifies the complexity of location of the cellular anatomy. The hippo thology. Figures 4—6show all of the fissures,
these cellular layers and makes this location campal sulcus (fissure) is presentin the head, the cellular anatomy of the hippocampus, and
ideal for evaluating the hippocampus. There body, and tail of the hippocampus.Anteriorly, its surrounding structures on colored serial
fore, hippocampal imaging is described in this fissure merges with the uncal sulcus [ 1]. coronal myelin-stained sections and on com
coronal sections that are perpendicular to the The hippocampal sulcus (fissure) is usually panion serial T2-weighted MR images.

@ k: :i Ch@

@ B

Fig.3.—Normal
coronalhippocampus in24-year-oldman.
A,Fastspin-echo12-weighted MRimagethrough bellyofponsshowschoroidal fissure(Ch),fimbriodentate
fissure(FD),andhippocampal sulci(H)(fissures)
onleft(also
seeFig.8A).Notethatsmallcysticresidualoffetalhippocampalsulcus(fissure)isseenonbothsides.
B,Fastspin-echo12-weightedMRimagethroughmiddlecerebellarpeduncleshowscontinuation ofthreemajorhippocampal sulci(fissures).Ch=choroidalfissure,
FD=fimbriodentatefissure,H =hippocampa)sulcus.Notesmallcysticresidualoffetalhippocampal sulcus(fissure)(solitaryarrowonrighthippocampus).

1140 AJR:171,October1998
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@,-#

@ . ,.

. —¿
Mama @arybodyd
Uncaf
:@ notch
(tertora@
@ r@press@on) S
@ Collateraf

C D

Choroidaf fia
- S Uncal guiCuS
r ‘¿@UncaI notch
.2 tentoraf
‘¿S Imoress;orr)

V Collateral
fissure
E
Dsntategynhs
—¿
—¿
entorhinal
area
(connects parahippocampus with CAl)

lanterlorparahlppocampalgyrus)

—¿
body
of
parahippocampal
gyrus
@ CA - @en.r
sictor) •¿ amygdala
Comu Ammonia
@ (Ammon's horn) :@:@.i.i“¿slat—It
zen.) gyms amblins
—¿
tail
of
parahippocampal
gyms
@
—¿ CM !.@::unaris —¿
vestigial
supracallosal
gyms
(becomes cingulate gyrusInot shown])

(induslum griseum)

Fig.4.—Normal
anatomyofamygdala
andhippocampal headonpairedserial,myelin-stained
coronalbrainsections
andcompanion
12-weightedMRimages.Bothmyelin-stained
sec
tionsandMRimagesareasymmetric,
causing
slightlydifferent
appearancebetween right-andleft-sided
structures,
whichproduces
sixuniquesections.
Colorkeyisguidetoimportant
structuresandlandmarks.
A,Myelin-stained
brainsectionimmediately
rostraltoheadofbothhippocampi.
B,CompanionMRimagerostraltohippocampishowsdivergingoptictract(Ot),sylvian
fissure(Sf),anduniquebranching
patternofwhitematterinrostraltemporal
lobeonrightRostral
amygdala(A)is seenonleft
C,Myelin-stained
brainsectionofanteriormost
lefthippocampal
headorpes(foot)showscornuammonis
zone1(CAl)belowtemporal
horn.Amygdala
(blue)persists
onrightbuthas
almostdisappearedonleftside.Uncus(pink)is seenaboveandmedialto bothamygdalae.Uncalnotchis postmortemartifact.
D,Companion MRimageshowsmamilothalamic tractsconvergingtositeofmamillary
bodies(Mb),sylvian
fissure(Sf),androstralrightamygdala
(A)asitfadesintouncus.Uncalrecess
(Ur)oftemporal
hornisseenonright(joinedarrows). UralsoisseeninE.
E,Myelin-stained
brainsectionofleftmidportionofhippocampal headorpes(foot)showsrelationshipofuncus(pink)toCAlcells(red).Notethatuncalextension oftemporal horn
seenonrightshouldnotbemistaken forpathology(Fig.10).Uncalsulcusisshownonleft CAlcellsseparateuncalsulcusfromuncalrecess.Righthippocampal headshowscompli
catedalternatingcellularrelationshipsof CAl (red),CA2(turquoise),andCA3(brightyellow)cellsto centrallylocatedamygdala(blue).CA4appearsin Figure5A.
1@
Companion
MRimageshowsinterpeduncularfossa
(If)between
cerebral
peduncles
andvessels
inambient
cistern(Ac)asitmerges
withchoroidalfissure
(Ch)andtemporal
horn(Th).
.-

•¿\4

Al F I
A4
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4'

@
@
, @----@- Choroidal
fissure fissure
Collateral fissure

—¿
Dentate
gyrus —¿
@ CA = @imer
sector) amygdala
—¿
entorhina)
area(connects parahtppocampus with CAl)

anterior parahlppocampat gyrus)


Comu Ammonia
—¿
body
of
parah(ppocampai
gyms
@ (Ammon's horn) @@iaI
rsslstant zone) gy@u@ambiens
—¿
tao
of
parahippocampa)
gyms
@
—¿
(End
folium)
CA3 @:@7unaris
—¿
vestigial
supracaliosa)
gyrus
becomescingulategyrus[notshown])

)induslum griseum)

Fig.5.—Normal
anatomy
ofhippocampal
bodyonpairedserial,myelin-stained
coronalbrainsections
andcompanion
12-weighted
MRimages.
Bothmyelin-stained
sections
andMR
imagesareasymmetric,causingslightlydifferentappearancebetweenright-andleft-sidedstructures,which producessixuniquesections.Colorkeyis guideto importantstructures
andlandmarks.
A,Myelin-stained brainsectionofbothanteriorhippocampal bodieshasclassiccellularconfigurationofcornuammonis zone1(CAl,red),zone2(CA2, turquoise),
zone3(CA3,bright
yellow),andthesmallest zone4(CA4, magenta) showninFigure 2.Largeportionofuncus(pink)continues tobepresent onrightbuthasalmostdisappeared onleftside.
B,Companion MRimageshowshypointense whitematterofalveus(Al)andfimbria(F),whichseparate hippocampal cortexbelowfromsuperior brightsignalintensity
ofpartialvolume
ofCSFandchoroidal plexusinthintemporal horn.Hypocellular
molecular layerofdentategyrus(arrowheads) hashypointense signalintensity
thatissameasthatseeninwhitematter
elsewhere inbrain.Imageisconfusing because intervening
cellsofcornuammonis zone2(CA2, turquoise)anddentate fibers(darkgreen)that separate hypointensealveusabovefrom
hypointense molecularlayerbelow(A)arenotresolved and,therefore, hypointensity
appears ascontinuous band.
C,Myelin-stained brainsectionofhippocampal bodyissmallerversionofclassiccellularconfigurationshowninA andinFigure2.UncalsulcusseeninA hasbecome hippocampal
sulcus(fissure),
andfimbriodentatefissurehasappeared. Atthislevel,cellsofentorhinal
area(lightgreen2)havebeenreplaced bymainbodyofparahippocampal gyrus(lightgreen2a).
D,Companion MRimageshowspulvinar (Pul)ofthalamus,choroidalfissure(Ch),collateral
fissure(CoIl),
andtemporal horn(Th)entering atriumoflateralventricle.
E,Myelin-stainedbrainsectionoflastportionofhippocampal bodyatantenormost splenium ofcorpuscallosum.Bodyofparahippocampal gyrus(lightgreen2a),whichispresentin
previous sections,
islastseenonthislevel.ItisreplacedinFigure 6Abytailofparahippocampal gyrus(lightgreen3).
F,Companion MRimage shows spleniumISpI),caudatenucleus )Cn),
andcrusoffornix )Cfx).
MR Imaging of the Hippocampus

@,if

* Sp:
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L @B
A

I
,@(tk,@@-
.‘

C D

—¿
Dentate
gynis —¿
@ CA @sn.r
sector) •¿ amygdaia
—¿
entorhinal
area(connects parahlppocampus with CAl)

(anterior parahippocampal gyrus)


ComuAmmonia
—¿
body
of
parahlppocampai
gyms
@ (Ammon'. horn) @@r@aI
nshetuit son.) gyi'tzs amblens
—¿
tail
of
parahippocampal
gyms
@ CA3 @::i@unai1s
—¿
vestigial
supracaiiosai
gyms
(becomes cingulate gyrus[not shown])

(indusiumgriseum)

Fig.6.—Normal
anatomyofhippocampal
tailonpairedserial,myelin-stained
coronalbrainsectionsandcompanion
12-weighted
MRimages.Bothmyelin-stained
sections
and MR imagesare asymmetric,causing slightly different appearancebetween right- and left-sided structures, which producesfour uniquesections. Colorkey is guide
to important structures and landmarks.
A,Myelin-stained
brainsectionofjunctionofbodyandhippocampal
tailbelowposteriorspleniumofcorpuscallosum.Cornuammonis
zone1(CAl)cells(red)predominate
and surround dentate gyrus (dark green).Gyrusfasciolaris is composedof CA3cells (yellow). Gyruscinerea is formed by CA4cells (magenta).Body of parahippocampal
gyrus (light green 2a in Figure5E)hasterminated, andtail of parahippocampalgyrus appears(light green 3). Collateralsulcus terminates at this level.
B,Companion MRimageshowsatriumof lateralventricle,anteriorcalcarinefissure(AC),andsplenium)Spl)of corpuscallosum.Alveus(Al)oftencanbeidentifiedbe
tweenbrightsignalintensityof CSFandcortexofcornuammonis zone1(CAl)hippocampal cells.
C,Myelin-stained
brainsectionofhippocampal tailcontainslastsmallremnantofcorpuscallosumbelowsupracallosal
gyrusonright.Anteriorcalcarinefissureseparates
cornu ammoniszones1 (CAl, red) and 3 (CA3,brightyellow) cellular layers of hippocampusfrom subiculum(light green 1).
D,Companion
MRimageshowsanteriorcalcarinefissure(AC).

MR lmagingTechniques field of view,256 x 256 matrix, 3- to 5-mm sec the limbic structures! Considerable disagree
Clinical1-lippocompalImaging tions with the smallest possible gap); and TI ment exists relating to how to perform these
High-field-strength MR ( I .5-T) scans are best weighted images (four repetitions, 16-cm field volumetric studiesand what the results mean.
suited fbr detailed hippocampal studies. All im of view, 3- to 5-mm contiguous sections). A Tl Currently, these studies are impractical in the
ages must use window settings that optimize weighted spoiled gradient-recalledecho in the routine clinical setting because highly trained
gray—whitematter differentiation. Excellent steadystate,inversionrecovery,or TI-weighted personnelmust trace the hippocampal outline.
quality standard axial images of the brain must fluid-attenuatedinversionrecoverysequencecan The details of this procedure have been re
be obtainedto detectconcurrentor separateab beobtainedifthese capabilitiesareavailable[6]. viewed recently [7].
normalities. However, the fbllowing coronal
scans of the hippocampus should also be ob- Volumetric
Analysis Spectroscopy
tamed: fast spin-echo T2- and spin density Over the last few years, more than 90 arti- MR spectroscopycan be usedto obtain non
weighted images (two repetitions. 20- to 24-cm des have described MR volumetric analysis of invasive biochemical information in a living pa

AJR:171, October 1998 1143


Hayman et al.

PC
Cr
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Cr

-,@. I,,., I

4 2 0
ppm
A B

Fig.7.—'HMRspectra.
A,Eightcubiccentimeters
ofnormal
frontoparietal
region.
Short-TE
(30msec)MRspectroscopy
showsgoodwatersuppression
andspectral
resolution
ofvarious
bio
chemicals.NAA= N-acetyl-L-aspartate,GABA=‘¿y-aminobutyric
acid, glu = glutamate,gIn= glutamine,asp= aspartate,PCr= phosphocreatine,Cr creatine, Cho= choline,
Ins= myo-inositol.
B,Fivecubiccentimetersof normalhippocampus.
Short-TE
(30msec)MRspectroscopy
showsbroaderspectralpeaksandpoorlydefinedbaselineresultingfromlocal
field inhomogeneitiesin region.Useof longerTE(>100msec)would significantly improvebaselineby increasingwater-suppressionefficiency. However,resulting spectral
information
wouldincludeonlyNAA,Cr,PCr,andChobecauseotherbiochemicals
haveshort12relaxationtimes.

. CAt2@

@ .,, / :‘@

@ . .. ., .. .p .
.,@ I

i@/P:,,:1@i1@::
A B

Fig.8.—Hippocampalsclerosis.
CAl=cornuammonis zone1.CA2= cornuammonis zone2.
A,Coronalsection ofbrainshowsnormal leftCA2andsevereatrophy ofleftCAlwithflattening
ofnormal
hippocampal bulgeintotemporalhorn(curvedarrow)(seenormal
coronalprofileinFig.2).Normalfissures(choroidal,Ch;fimbriodentate,
FD;andhippocampal, H)aremarkedfororientation.
B,Microscopiccoronalsectionofbodyofhippocampus showsclassiclossofcellsinCAlofhippocampuscompared withnormaldarktriangularpyramidalcells(arrows)
in CA2region.(HandE,xlOO)

tient and has been performed in an effort to crowded under optimal conditions, magnetic Refractory Epilepsy
detect early onset of Alzheimer's disease and to field inhomogeneities caused by the bone or air Epilepsy affects 0.5—1%of the population in
study normal age-associated memory impair interfaces(or both) near the hippocampuspro the United States.Of theseindividuals, 15—30%
ment. MR spectroscopy may be of particular ducebroadenedspectralpeaksand makequan are refractory to medical treatment and are po
importance in patients with a normal MR scan titative analysis difficult [7] (Fig. 7). However, tential candidates for surgical resection [8].
and medically intractable epilepsy [7]. How the useof small voxel sizes,obtainedwith spec Electroencephalographicstudies are the most
ever, the clinical usefulness of this technique in troscopicimaging techniquescoupledwith effi important localizing tools in these patients. If
studiesof the limbic systemhasbeenlimited by cient magneticfield homogeneityoptimization, imaging shows hippocampal sclerosis at the site
many technical pitfalls. For example, in 1H MR may expand the clinical applications of MR of a temporal lobe electroencephalographicab
spectroscopy, in which the spectral peaks are spectroscopyin the limbic system. normality, the surgical outcome is greatly im

1144 AJR:171,October1998
,@“ I .1
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,1 I

A B

Fig.9.—Hippocampal
sclerosis.
A,Coronalfastspin-echo12-weighted
scanshowsabnormal increasedsignalintensity
inbodyoflefthippocampus (arrow)compared withnormal rightside.
B,Coronalfastspin-echo12-weighted
scancaudalto A showsthatatrophyof hippocampus
onleftresultsin subtleincreasedsizeof leftchoroidalfissure(Ch)(arrow).
Normalthinner choroidal fissure on right side also is markedwith arrow for comparison.

Fig.10.—Fibrillary
astrocytoma.
A,Coronalfastspin-echo 12-weighted
scanshowsabnormal
focusofincreased
signalintensity
atjunction
ofrightamygdala
andhippocampal
head(arrow)(seeFig.4C,
left hippocampalsection).This finding should not be mistakenfor uncal recess of temporal horn (see Figs.4D and 4E).
B,Companion
11-weighted
imagesbefore(notshown)andaftergadolinium
administration
donotshowabnormality.

proved (i.e.. 8()—9O@7c


of these individuals
becomeseizure-free).This finding is significant
becauseone half of patientswith medically in
tractableseizureshavehippocampalsclerosis.
MR imaging is the technique of choice in
@¼@#@fT 7:
these patients because it has a 90% sensitivity
to hippocampal sclerosis,whereasCT is sensi
tive in only 2% of cases (Figs. 8 and 9). MR
imaging also is superior to CT in the detection
of other causesof refractory epilepsy, such as
congenital deformities, low-grade tumors (Fig.
tu
10), trauma, stroke, and infections. Recogni
tion that scalp electroencephalographsmay
falsely localize an abnormality to the hippo
campus is important. In this setting, imaging is
of utmost importance becauseit can prompt
Fig. 11.—Temporal
lobe ganglioglioma.Fastspin-echo 12-weighted image shows left inferior temporal lobe le
the use of depth electrodes to correctly localize sion(arrow)thatwasnotseenonunenhanced
11-weightedscans.Scalpelectroencephalograph
erroneously
the causative lesion (Fig. 1 1). indicated focus in oppositetemporal lobe. Subduralelectrodes correctly localized lesion.

AJR:171,October1998 1145
Hayman et al.

Summary true coronal brain slices. We are extremely 4. FullerGN,BurgerPC.Centralnervoussystem.In:


grateful for the expertise and patience provided Sternberg
SS,ed.Histologyfor pathologists,
2nd
The hippocampus is a complex and fasci
ed.NewYork:Lippincon—Raven,
1997:243—282
nating region of the brain that has enormous for this undertakingby BrendaSchubert.
5. Tien RD. FelsbergGJ. Cram B. Normal anatomy
clinical significance. Specifically, small imag of the hippocampusand adjacenttemporallobe:
ing abnormalities may cause major symp References high-resolution
fastspin—echo
MR imagesin vol
toms. We believe that the detection of these 1. DuvernoyHM. The humanhippocampus: an at unteerscorrelatedwith cadaverichistologicsec
las of applied anatomy. Munich: Bergmann Ver tions. AiR 1992;l59: 1309—1313
Downloaded from www.ajronline.org by 92.83.162.251 on 11/29/22 from IP address 92.83.162.251. Copyright ARRS. For personal use only; all rights reserved

lesions will be improved if imaging clinicians


lag,1988:1—45 6. Jack CR, Rydberg CH, Krecke KN, et al. Mesial
have an organized reference that facilitates
2. BronenRA, Cheung0. Relationshipof hippo temporalsclerosis:diagnosiswith fluid-attenu
identification of the cellular zones that com campusandamygdala
tocoronalMRI landmarks. ated inversion-recoveryversusspin-echoMR im
prise the hippocampus. Magn Reson Imaging 1991:9:449—457 aging. Radiology 1996;l99:367—373
3. Naidich TP, Daniels DL, Haughton VM, Williams 7. Tien RD. Neuroimaging clinics of North Amer
A, Pojunas K, PalaciosE. Hippocampalforma ica: the limbic system normal anatomy and pa
Acknowledgments tion and related structures of the limbic lobe: ana thologv. Philadelphia: Saunders, 1997
We thank the Armed ForcesInstitute of Pa tomic—MRcorrelation. 1. Surface features and 8. Jack CR. Magnetic resonance imaging in epi
thology, Washington, DC, for providing the coronal sections. Radiology 1987;l62:747—754 lepsy.MayoClinPmc 1996;7l:695—711

1146 AJR:171,October1998

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