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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2821_Библиотеки_им_академика_М_И_Перельмана
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CHAPTER13•CongenitalFoot,Ankle,andLowerExtremityConditions
TylerA.GonzalezandRaymondHsu
CHAPTER14•EndocrineDisordersPresentingintheLowerExtremity
DanielGuss
CHAPTER15•DermatologicManifestationsofSystemicDiseaseintheLowerExtremity
SharonR.Barlizo,ThomasM.Delauro,andMarkLebwohl
CHAPTER16•LaboratoryEvaluationofSystemicRheumaticDiseasesintheLower
Extremity
BellaMehtaandStevenK.Magid
CHAPTER17•MetabolicBoneDiseaseManifestationsintheFoot
PanagiotaAndreopoulou
CHAPTER18•Gastrointestinal/HepaticDiseaseManifestationsintheLowerExtremity
BrianP.BosworthandYecheskelSchneider
CHAPTER19•AcuteEmergenciesRelatedtoSystemicDiseaseandHowTheyPresentin
theLowerExtremity
EdwardAmoresandRahulSharma
CHAPTER20•FootUlcersAssociatedwithHematologicDisorders
LeonardA.Levy
CHAPTER21•LowerExtremityManifestationsofSpineDisease
SravishtIyerandToddJ.Albert
CHAPTER22•LowerExtremityTendinopathyintheSettingofSystemicDisease
AndrewJ.Rosenbaum,JasonP.Tartaglione,MostafaAbousayed,MaxwellC.Alley,andJoshuaS.Dines
CHAPTER23•PedalandLowerExtremityManifestationsofHIV
KhurramH.Khan,GeorgeS.AbdelmessiehandRihamM.Wahba
CHAPTER24•FootComplicationsofObesity
LouisJ.Aronne,AnthonyCasper,RekhaKumar,LeonIgel,andAlpanaShukla
CHAPTER25•LowerExtremitySignsandSymptomsofMultipleSclerosis
MaryAnnPicone,HunterVincent,KarenBlitz-Shabbir,CloverYounWest,andJemimaAkinsanya
Index
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SystemicDisease
Manifestationsin
theFoot,Ankle,and
LowerExtremity
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T
he foot and ankle are constantly being stepped on and stressed by both normal and
extraordinaryforces.Feetaretakenforgranted,untiltheyarehurt,limitambulation,make
wearing shoes difficult, cause gait disturbances, or some other malady forces the foot
and/or ankle to take on a new level of importance. Most of the time, foot conditions are
localizedtoa bunion,flat foot, or Achilles tendon injurythat canbe treated withorthotics,
change of footwear, exercises, local injection, or a combination of these therapies and/or
surgery.Onotheroccasions,footand/oranklepainandabnormalitiesofthelowerextremity
mayresultfromanunderlyingsystemiccondition.Whenreviewingimagingexaminations,for
example, radiographs (X-ray), magnetic resonance imaging (MRI), ultrasound, or
computerized tomography (CT) examinations of the lower extremity, possible underlying
systemic conditions must be considered. Familiarity with systemic conditions that can be
identified on an imaging examination facilitates early diagnosis and intervention. These
conditions fall into the classic categories of arthritis, infection, tumor, vascular,
developmental,metabolic,andother.Inthischapter,theimagingfindingsofvarioussystemic
conditionsthatcanpresentwithchangesinthelowerextremityareorganizedalphabetically.
FIBROUSDYSPLASIA
Fibrousdysplasiaisasporadicbonediseaseinwhichbenignfibro-osseouslesionsdevelop
during skeletal formation.1 Occasionally, fibrous dysplasia can arise as a component of
McCune–Albright syndrome or Mazabraud syndrome.2 Lesions can occur anywhere on the
skeleton, with thecraniofacialbones, ribs,andlongbonesmostcommonlyinvolved.1In the
lowerextremity,thefemurandtibiaaremostoftenaffected.1Fibrousdysplasiaoccursinboth
monostotic andpolyostotic forms, with theformer accounting for approximately80% ofall
cases.2 Often asymptomatic, fibrous dysplasia is diagnosed incidentally on radiographs
obtainedforunrelatedreasons.1Insuchcases,notreatmentisneeded.1Thepolyostoticformis
morelikelyto producesymptoms includingpain,limp,anddeformity, andlargelesions are
prone to pathologic fracture.1 Rarely, fibrous dysplasia is complicated by malignant
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degeneration,particularlyinpreviouslyirradiatedareas.
1
FIGURE1-1.Radiographicpatternoffibrousdysplasia.FrontalX-rayofthelowerextremities(A)andleftfemur
(B)demonstratesexpansilelesionswithcharacteristicgroundglassmatrix,thincortices,andbowingdeformities.
Notatypically,polyostoticfibrousdysplasiaaffectsonesidemorethantheother.
Fibrous dysplasia demonstrates a characteristic radiographic appearance of
intramedullary, well-defined, and expansile lesions with a radiolucent “ground glass”
matrix.
1,2
Shepherd’scrookdeformityoftheproximalfemurisalateralbowingdeformityand
coxa vara.2 Saber shin deformity is an anterior bowing deformity of the tibia commonly
associatedwithfibrousdysplasia(Fig.1-1).
GOUT
Gout, aninflammatory arthritis, is a crystal arthropathy characterizedby hyperuricemia and
subsequentdepositionofmonosodiumurate(MSU)crystalsinjointsandsofttissues.3Goutis
acommon andpotentiallydebilitatingcondition,disproportionatelyaffectingmen.3 Affected
individuals experience recurrent acute inflammatory flares as well as chronic destructive
changessecondarytoMSUcrystaldeposition.Goutcaninvolveanyjointbutmostfrequently
affects the feet, demonstrating a predilectionfor the 1st metatarsophalangeal (MTP) joint.
4
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Gout can be associated with metabolic syndromes, myocardial infarction, and diabetes
mellitus.
Radiographs of involved joints may reveal marginal “punched out” erosions, sclerotic
margins,andoverhangingedges,withrelativepreservationofthejointspace;however,X-ray
changestypicallyoccurlateinthecourseofthedisease.
3,4
Radiographsmayalsodemonstrate
macroscopicdepositionsofMSU crystals,ortophi,whichareahallmark featureofchronic
gout.4Tophimaybeperiarticularorintra-articular;CTisparticularlyusefulindetectingintraarticular depositions.4 Tophi display intermediate or low signal on T1-weighted MRI
sequences, with variable appearance on T2-weighted sequences.3 Postcontrast sequences
generally demonstrate enhancement, and there is often associated synovial thickening and
adjacent marrow edema.
3,4
MRI can also reveal erosions before they become visible on
radiographs(Fig.1-2).
4
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FIGURE1-2.RadiographicandMRpatternsofgout.AandB:Frontalandobliqueradiographsofthefootin
differentpatientswithgout.A:FrontalX-rayofthefootdemonstratesmedialsofttissueprominenceofgoutytophus
adjacenttothemetatarsalheadofthegreattoewithoutunderlyingboneorjointabnormalities.B:ObliqueX-rayview
demonstratesclassic“overhangingedge”ofgoutatthemedialandlateralaspectsofthemetatarsalheadofthe
greattoe.CtoE:MRdemonstrationofgout.C:CoronalfastspinechoMRimageofthe1stMTPjointdemonstrates
theheterogeneouslyhyperintensesofttissuemassofgoutytophusmedialtothe1stMTPjoint.D:Coronalfastspin
echoprotondensity-weightedimagedemonstratesaheterogeneousexpansilehyperintensemassofgoutytyphus
circumferentiallyaboutthe3rdPIPjoint.E:Axialfastspinechoprotondensity-weightedimagethroughtheforefoot
demonstratesfocalheterogeneouslyhyperintensesofttissuetophuswithintheplantarmarginsofboththe1stand
3rdMTPjoints.Thesofttissuetophusaboutthe3rdMTPjointextendsdorsally.
HYPERTROPHICPULMONARYOSTEOARTHROPATHY
Hypertrophic pulmonaryosteoarthropathy(HPO)orPierreMarie–Bambergersyndrome isa
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syndrome of unknown etiology characterized by the triad of periosteal bone deposition,
clubbingofthedigits,andarthralgia,whichoccursinassociationwithpulmonarypathology.
5,6
HPO can develop in many chronic pulmonary conditions, but in the majority of cases is
associatedwithprimarylungmalignancies.5Rarely,patientswithextrathoracicdiseasessuch
as inflammatory bowel disease can develop HPO.5 Patients typically present with pain,
tenderness,and swelling.Radiographsdemonstrate generalizedperiostealreactionalong the
diaphyses and metaphyses of long bones sparing the epiphyses.6 MRI can be helpful in
demonstratingadjacentsofttissueswellingandmuscularedema(Fig.1-3).
6
INFARCTANDOSTEONECROSIS
Osteonecrosisandboneinfarctdefinebonedeath.Osteonecrosisistypicallyusedtodescribe
ischemicbonedeathinasubchondrallocation,andboneinfarctisusedwhenthelesionisnot
in a subchondral location. Systemic causes of bone death are corticosteroids, sickle cell
anemia, collagenvascular disease, alcoholism, andidiopathic.7 Themost common cause of
osteonecrosis in a subchondral location istrauma thatpresents as mixedlytic andsclerotic
areas on radiographs and that can progress to microfractures in articular collapse if left
untreated.
8
FIGURE1-3.RadiographicpresentationofHPO.A:X-rayoftherightankledemonstratesthickperiosteal
reactionatthedistalaspectofthelongbone,sparingtheepiphysis(arrow)withoutunderlyingbonepathology.
Posteroanterior(PA)radiographofthechest(B)inthesamepatientdemonstratesalarge,leftupperlobelesion.
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Infarctsinthelowerextremityoccurprimarilyinthemedullarycavityofthelongbones.
8
On radiographs,infarctspresentasan elongatedserpiginous rimofsclerosis witha central
lucency. MRI is the most sensitive test for suspected bone infarct and demonstrates
characteristicfindings.7The lesionscontainacenterofdevitalizedmarrow surroundedbya
rimofgranulationtissueandsclerosis,whichgivestheselesions a centralhigh signalfrom
adipose marrow with a surrounding ring of hyperintense inner granulation tissue and
hypointenseouterringofsclerosisandisclassicallyreferredtoasthe“double-line”sign(Fig.
1-4).
MAFFUCCISYNDROME
Maffucci syndrome is a nonhereditary and rare dyschondroplasia of unknown origin
characterized by multiple enchondromas combined with soft tissue venous malformations.
9
Enchondromasarebenigncartilaginouslesionswithinthemetadiaphysisoftubularbonesthat
typically present as osteolytic expansile lesions with central stippled calcifications
characteristicofachondroidmatrix(Fig.1-5).
10
MELORHEOSTOSIS
Melorheostosisisanuncommonsclerosingbonedysplasia ofunknownetiology.
11,12
Patients
areusuallyasymptomaticbutcanpresentwithlimbstiffnessorpain.11Thetypicalappearance
onradiographsisofflowinghyperostosisalongtheoutercorticalsurfaceofthelongbonesof
the lower extremity, which usually has an undulating appearance, referred to as “dripping
candlewaxsign”(Fig.1-6).
11
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FIGURE1-4.X-rayandMRfindingsofboneinfarct.A:LateralX-rayoftheankledemonstratesaclassicbone
infarctwithanirregularserpiginouselongatedlucencyinthedistaltibiawithoutperiostealorendostealreaction
(arrow).Sagittalinversionrecovery(B)andprotondensity-weightedimages(C)demonstratethecharacteristic
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heterogeneouslyhyperintenseserpiginouspatternofboneinfarctonMRI.
METASTATICDISEASE
Boneisacommonsiteofmetastaticinvolvementinmalignancy.13Manyprimarymalignancies
can metastasize to the skeleton; however, breast, prostate, and lung carcinoma are most
frequentlyassociatedwithosseousinvolvement.13Lessfrequently,kidneyandthyroidcancers
metastasizetothebone.Metastaticlesionscanbepainfulandmayleadtopathologicfractureif
extensive cortical destruction is present.14 The axial skeleton and proximal long bones are
disproportionatelyaffectedinmetastaticdisease,inpartbecauseofthehigherrelativecontent
ofvascularizedredmarrow.
14
The radiographic appearance ofosseousmetastases dependson the primarymalignancy
andtheboneresponseelicitedbythemetastaticdeposit.13Breastandlungcarcinomatypically
producemixedlyticandblastic lesions.13Lyticlesions are characterizedby excessive bone
resorption andare often seenwith thyroid andrenal carcinoma, whereas blastic (sclerotic)
lesions,characterizedbyexcessiveboneformation,areoftenseenwithprostatecarcinoma.
13
Radiographic features associated with osseous metastases include poorly defined margins,
endostealscalloping,corticaldestruction,andperiostealreaction.Anextraosseoussofttissue
componentmayoccasionallybeassociated(Fig.1-7).
14
FIGURE1-5.RadiographicmanifestationsofMaffuccisyndromeintwoseparatepatients.A:Standing
anteroposterior(AP)examinationofthelowerextremitiesdemonstratesnumerousdeformingenchondromas
throughouttherightlowerextremityinvolvingthetibia,fibula,femur,andthepelvis.Asymmetricdistributionis
common,withupto50%oflesionsbeingunilateral.9B:Lateralviewoftherighttibiaandfibulademonstratessoft
tissuecalcificationsrepresentativeofvenousmalformationanteriortothekneeandtibia.C:APofthefoot
demonstratesclassiccalcifiedvenousmalformationsinthesofttissuesandscallopingofthemetatarsals.The
enchondromasarelessevidentinthefootofthispatient.
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