Robbins Essential Pathology p137-142 PDF
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Summary
This document discusses diseases of blood vessels, including vasculitis and giant cell arteritis. It covers pathologies, clinical features, and potential causes.
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112 CHAPTER 7 Diseases of Blood Vessels erapy, and surg c a rep a r o e aor c n ma e ar c an s ave 65% Pathogeness. he carac...
112 CHAPTER 7 Diseases of Blood Vessels erapy, and surg c a rep a r o e aor c n ma e ar c an s ave 65% Pathogeness. he caracersc granuomaous nlammaon, an asso- o 85% o e p a ens w d ss e c on nvov ng e aor c arc. Ds - caon w ceran HLA cass II apoypes, and e exceen era- s e c ons a do no nvove e aor c arc c an be re p a re d surg - peuc response o serods a suppor an mmune eoogy. Gan ce c a y or manage d c ons er va vey w an y p e r ens ve d r ugs and arers key occurs as a resu o a cronc h1 ce–medaed mmune ave s ome w a b eer oucomes. response, presumaby o angens presen n e vesse wa. he deny o ese angens and e bass or e predecon or vesses o e ead are unknown. VASCULITIS Vasculitis encompasses a group of disorders with highly varied Morphology. Granu omaous nl amma on o cc urs n a p acy pathophysiology and clinical features that are dened by the pres ds r bu on a ong e eng o afe c e d vess es. Invove d ar er a ence of vessel wall inammation. s eg mens exb no du ar n ma ckenng (and o cc asona Cnca manesaons depend on e specc vascuar bed a romb os es) a mpnge on e umen and c aus e ds a s cem a. s afeced and somemes ncude sgns and sympoms o sysemc Fu y de veop e d esons conss o nonne cro zng g ranu omas nlammaon. Many orms o vascus are recognzed, some w w mu nuce ae d g an ce s cenere d on e ner na e as c overappng eaures. Eoog y s dverse and ncudes mmune-me- membrane, w c s oten rag mene d (Fg. 7.10). He a ng o daed nlammaon, necons, drugs and cemcas, radaon e njur y s ass o c ae d w n ma ckenng , nnng and exposure, and rauma. I s crca o dsngus necous rom s c ar r ng o e me d a, and adven a bross. mmune-medaed orms because mmunosuppressve erapy s approprae or e aer bu coud exacerbae necous vascus. We w resrc our dscusson o orms o vascus a are mos com- Clncal Features. Gan ce arers s e mos common orm o vas- mon or o greaes paogenc neres, sarng w ose a prmar- cus among oder adus n ger-ncome counres. I s rare beore y afec arge vesses. 50 years o age. Sgns and sympoms may relec sysemc nlamma- on (ever, maase, weg oss) or ake e orm o aca pan or Giant Cell (Temporal) Arteritis eadace, mos nense aong e empora arer y, wc s panu o Giant cell (temporal) arteritis is a chronic granulomatous disorder papaon. Ocuar sympoms appear abrupy n abou 50% o paens that principally affects large-sized arteries in the head. and range rom dpopa o compee vson oss. Dagnoss requres he empora, verebra, and opamc ar eres and e aora can bopsy, ypcay o e empora arer y ; owever, because e arers be nvoved. Opamc ar er y nvovemen can cause sudden and s pacy, a negave bopsy resu does no excude e dagnoss. Cor- permanen bndness; ereore, promp dagnoss and reamen are coserod or an–umor necross acor (TNF) erapes are efecve essena. reamens. A B Fig. 7.10 Giant cell arteritis. (A) Hematoxylin-and-eosin (H&E)–stained section of a temporal artery showing giant cells near the fragmented internal elastic membrane (arrow), along with medial and adventitial inflamma- tion. (B) Elastic tissue staining demonstrating focal destruction of the internal elastic membrane (arrow) and associated medial attenuation and scarring. CHAPTER 7 Diseases of Blood Vessels 113 Takayasu Arteritis bu oers become quescen ater 1 o 2 years and are compabe w Takayasu arteritis is a granulomatous vasculitis of large-sized ong-erm sur vva, abe w vsua or neuroogc decs. arteries characterized by ocular disturbances and weakened Polyarteritis Nodosa pulses in the upper extremities. Takayasu arers maness w ransmura scarrng and cken- Polyarteritis nodosa is a systemic vasculitis of medium-sized mus- ng o e aora—parcuary e aorc arc and grea vesses—and cular arteries that commonly involves renal and visceral vessels umna narrowng o e major branc vesses. Is eaures overap w and usually spares the lung. ose o gan ce arers e dsncon beween e wo enes s made argey on e bass o a paen’s age, w ose younger an 50 Pathogeness. he cause o poyarers nodosa s unknown, bu years o age beng desgnaed as avng Takayasu arers Lke gan e dsease responds we o mmunosuppressve agens and ere- ce arers, Takayasu arers appears o be caused by a cronc gran- ore s beeved o ave an mmunoogc bass. One rd o paens uomaous T-ce–medaed mmune response o an unknown vesse ave cronc epas B necon and may ave crcuang mmune angen. compexes composed o vra angens and specc anbodes, wc depos n vesse was and provoke an nlammaor y response. Wy mmune compexes ocaze n medum-szed areres and no n oer Morphology. he aora, e aorc arc, and s brances, as we as vesses s unknown. e pumonar y, rena, and coronar y areres, may be afeced. he akeofs o e grea vesses may be narrowed or oberaed (Fg. Morphology. Vesses o e kdney, ear, ver, and gasronesna 7.11), eadng o upper exremy weakness and an carod puses. rac vesses are afeced n descendng order o requency. Inlammaor y nraes n vesse was range rom nonspecc Fuy deveoped esons are composed o segmena ransmura accumuaons o T ces and macropages o granuomaous necrozng nlammaon o medum-szed or, occasonay, sma nlammaon, bo o wc may be assocaed w wa ckenng areres, oten w supermposed romboss. Acue esons ave and bross. brnod necross o e vesse wa and nrang neurops (Fg. 7.12), wereas oder esons are broc and assocaed w cronc Clncal Features. Invovemen o e aorc arc and major brances nlammaon. Acue and cronc esons coexs, suggesng produces reduced upper-exremy bood pressure and puse sreng, ongong recurren nlammaor y damage. he vascuar njur y may neuroogc decs, vsua ed deecs, and bndness. Sympoms mpar e peruson o downsream ssues, eadng o uceraons, reaed o nvovemen o e dsa aora (eg caudcaon), e pu- narcs, and scemc aropy, or may provoke aneur ysm ormaon monar y arer y (pumonar y yperenson), e ear (myocarda and e aendan rsk o emorrage. narcon), and e rena areres (sysemc yperenson) aso may appear. he dsease as a varabe course. Some cases rapdy progress, Clncal Features. Poyarers nodosa s more common n young adus bu can occur a any age. he cnca course ypcay s epsodc, w ong sympom-ree ner vas. Ina sympoms—maase, ever, and weg oss—are reaed o nlammaon and are nonspecc, and e vascuar nvovemen s vared and may be wdey dsrbued, eadng o puzzng, proean manesaons suc as yperenson due o rena arer y nvovemen and abdomna pan and boody soos caused by gasronesna esons; dfuse muscuar aces and pans; and perp- era neurs, predomnany afecng moor ner ves. Rena nvovemen s a major cause o dea. Unreaed, poyarers nodosa s usuay aa, A B Fig. 7.11 Takayasu arteritis. (A) Aortic arch angiogram showing reduced flow of contrast material into the great vessels and narrowing of the brachiocephalic, carotid, and subclavian arteries (arrows). (B) Cross sec- Fig. 7.12 Polyarteritis nodosa, associated with segmental fibrinoid tions of the right carotid artery from the patient shown in (A) demon- necrosis and thrombotic occlusion of a small artery. Note that part of the strating marked intimal thickening and luminal narrowing. The white vessel (upper-right, arrow) is uninvolved. (Courtesy Sidney Murphree, circles correspond to the original vessel wall; the inner core of tan tissue MD, Department of Pathology, University of Texas Southwestern Med- is the area of intimal hyperplasia. ical School, Dallas.) 114 CHAPTER 7 Diseases of Blood Vessels bu w mmunosuppressve erapy remsson or cure s aceved n res—probaby due o nvovemen o nerves. I e paen connues o 90% o cases. smoke, cronc uceraons may deveop and progress over me o gan- grene. Smokng absnence can a progresson, bu once esabsed, Kawasaki Disease e vascuar esons do no rem w smokng absnence. Kawasaki disease is an acute, febrile, self-limited illness of infancy Small-Vessel Vasculitides and childhood associated with an arteritis of large- to medium- sized vessels. Many oer orms o vascus prmary afec sma vesses. Aoug Is cnca sgncance sems rom requen nvovemen o coro- er paogeness s ncompeey undersood, wo groups ave emerged: nar y areres. Antneutrop cytopasmc antbody (ANCA)–assocated vascu- tdes. hese vascudes are dened by e presence o auoan- Pathogeness. he cause o Kawasak dsease s unknown. he dsease bodes agans varous componens o neurop granues. here sows a seasona varaon n ncdence, suggesng a a vra nec- are wo orms o ANCA: (1) an-proenase-3 ANCA (ormery on rggers an mmune response a njures areres secondary. reerred o as c-ANCA), dreced agans PR-3, a neurop azuro- pc granue consuen (PR3-ANCA); and (2) an–myeoperox- Morphology. he vascus resembes a seen n poyarers dase ANCA (ormery reerred o as p-ANCA), dreced agans nodosa, aoug brnod necross s usuay no as promnen. a neurop ysosoma enzyme, myeoperoxdase (MPO-ANCA). Afeced vesses ave a dense ransmura nlammaor y nrae a Severa orms o ANCA-assocaed vascudes are recognzed w ncudes neurops and mononucear ces. I et unreaed, damage paray overappng eaures. hey ncude PR3-ANCA posve caused by e nlammaon may ead o aneur ysm ormaon. granuomaoss w poyangs and MPO-ANCA posve mcro- scopc poyangs. Bo are assocaed w gomeruoneprs and Clncal Features. Kawasak dsease ypcay maness w conjuncva pumonar y dsease, requeny eadng o emopyss. I s uncear and ora eryema accompaned by bserng, eryema and edema o e e ANCAs ave a drec paogenc roe, bu ese anbodes are ands and ee, a desquamave ras, and cervca ymp node enarge- presen n a g racon o afeced paens and ereore are o men. Approxmaey 20% o unreaed paens ave cardovascuar com- dagnosc vaue. Treamen s w mmunosuppressve agens. pcaons, mos noaby e deveopmen o coronary arery aneurysms, Immune-compex, sma-vesse vascutdes. hese vascudes are wc may rupure or rombose, eadng o myocarda narcon and/ caracerzed by mmunogobun and compemen deposon or sudden dea. he dsease responds we o annlammaory agens a e ses o vascuar njur y. Anbodes may bnd drecy o (speccay, nravenous mmunogobun and asprn), wc sarpy componens o e vesse wa or be deposed as par o mmune reduce e ncdence o sympomac coronary arery dsease. compexes, or exampe n assocaon w sysemc upus er ye- maosus. he dsrbuon o vascuar njur y and e resuan cn- Thromboangiitis Obliterans (Buerger Disease) ca ndngs dfer dependng on e naure o e auoanbodes or Thromboangiitis obliterans is a severe form of vasculitis that is mmune compexes. In sysemc upus er yemaosus and Good- strongly associated with tobacco smoking. pasure syndrome, e kdney s severey afeced (see Caper 11). I prmary afecs sma and mdde-szed areres o e arms and Infectious Vasculitis egs, and oten produces severe scema, uceraons, and gangrene and ampuaon o afeced ssues. Drec vascuar nvason by necous agens, usuay bacera or ung, parcuary Pseudomonas, Aspergus, and Mucor spp, may cause Pathogeness. Bo e naon and progresson o romboangs ocazed arers. Vascuar nvason can be par o a ssue necon oberans depend on exposure o obacco smoke, bu e precse roe o (e.g., bacera pneumona or adjacen o abscesses), or, ess commony, smokng s uncear. One dea s a some componen o obacco smoke may arse rom emaogenous spread o bacera durng sepcema drecy damages e endoeum and a e vascuar canges are due or embozaon rom necve endocards. Vascuar necons can o drec oxcy. Aernavey, a reacve compound n obacco smoke weaken arera was suiceny o cause aneur ysms (mycotc aneu- may mody vesse wa componens and nduce an mmune response. rysm) or can nduce romboss and narcon. Ceran HLA-ypes are more suscepbe, conssen w a roe or mmune njury. Ceran enc groups (Israe, Indan subconnen, Jap- DISORDERS OF VEINS anese) are aso a greaer rsk, ponng o one or more genec acors. Varcose vens and rombopebs accoun or a eas 90% o cn- cay reevan venous dseases. Morphology. Caracerscay, ere s segmena acue and cronc ransmura vascus o medum- and sma-szed areres, Varicose Veins predomnany n e exremes. In e eary sages, mxed Varicose veins are abnormally dilated tortuous veins produced by nlammaory nraes, wc may gve rse o mcroabscesses, are chronically increased intraluminal pressures and weakened vessel accompaned by umna romboss. he nlammaon oten exends wall support. no conguous vens and nerves (a eaure rarey seen n oer orms Venous daon can occur a mupe ses: o vascus). W me, romb organze and evenuay e arery Varcose vens o e exremes occur n up o 20% o men and one and adjacen srucures become encased n brous ssue. rd o women; obesy and pregnancy ncrease e rsk. hey mos commony afec e superca vens o e egs. Varcose daon renders e venous vaves ncompeen and eads o ower-exremy Clncal Features. Paens are usuay younger an 45 and ave a sass, congeson, edema, pan, and romboss. Perssen edema smokng sory o more an 20 pack-years. hromboangs ober- and secondar y scemc skn canges may ead o sass dermas ans may presen w Raynaud penomenon, nsep oo pan nduced and uceraons, wc oten ea poory and are prone o superm- by exercse, or superca noduar pebs (venous nlammaon). he posed necon. vascuar nsuicency ends o be accompaned by severe pan—even a CHAPTER 7 Diseases of Blood Vessels 115 Esopagea varces may arse n e seng o pora yperen- Capary emangomas are e mos common ype; ese occur n son secondar y o ver crross and (ess requeny) pora ven e skn, subcuaneous ssues, and mucous membranes o e ora obsrucon or epac ven romboss (see Caper 13). Esop- caves and ps, as we as n e ver, speen, and kdneys (Fg. agea varces are one o severa ypes o porosysemc suns a 7.13A). Hsoogcay, ey are composed o n-waed capares may appear w pora yperenson; oer common ses o sun- w scan sroma (Fg. 7.13B). ng ncude e reca vens (emorrods, descrbed beow) and e Juvene emangomas (so-caed strawberry emangomas) o e perumbca vens (producng wa s known as caput medusa, a newborn are common (1 n 200 brs), nvove e skn, and may ancu erm or e magned resembance o e daed snake- be mupe. hey grow rapdy, bu mos regress compeey. ke vens o e ead o Medusa). Esopagea varces are cncay P yogenc granuomas manes as rapdy growng, red peduncu- sgncan because ey are prone o rupure, eadng o massve, aed esons on e skn or gngva or ora mucosa a beed easy somemes aa upper gasronesna emorrages. and are oten uceraed. Mcroscopcay, ey resembe exuberan Hemorrods are varcose daons o e venous pexus a e ano- granuaon ssue (Fg. 7.13C). reca juncon. hey resu rom proonged pevc vascuar conges- C avernous emangomas are composed o arge, daed vascuar on, mos commony due o pregnancy or sranng o deecae. cannes (Fg. 7.13D). C ompared w capar y emangomas, Hemorrods are a source o beedng and are prone o romboss cavernous emangomas are more nrave, requeny nvove and panu uceraon. deep srucures, and do no sponaneousy regress. hey may be ocay desrucve; surgca excson may be requred n some Thrombophlebitis cases. Cavernous emangomas are one componen o von Hp- Thrombosis of deep leg veins accounts for more than 90% of cases pe-Lndau dsease (Caper 17), n wc vascuar esons are of thrombophlebitis and is the source of most pulmonary emboli. commony ound n e cerebeum, bran sem, rena, pancreas, Oer ses were deep venous romb may orm are e perpros- and ver. ac venous pexus n maes and e pevc venous pexus n emaes, as Kaposi Sarcoma we as e arge vens n e sku and e dura snuses (especay n e seng o necon or nlammaon). Peronea necons and cer- Kaposi sarcoma is a vascular neoplasm caused by human her- an condons assocaed w ypercoaguaby (e.g., poycyema pesvirus-8 (HHV-8, also known as Kaposi sarcoma herpesvirus vera; see Caper 9) may ead o pora ven romboss. [KSHV]). Kapos sarcoma (KS) s mos common n ndvduas w mpared Pathogeness. hromboss s reaed o one or more componens o e T-ce uncon. Four orms o KS, based on popuaon demograpcs Vrcow rad: low abnormaes, endoea njury or dysuncon, and rsks, are recognzed: and ypercoaguaby (see Caper 3). Proonged mmobzaon a C a ss c KS o cc urs n o d e r men o Me d e r r an e a n , M d d e resus n venous sass (e.g., exended bed res n e possurgca sae, E aser n, or E aser n Eu rop e an d e s c e n ( e sp e c a y As ke n a z or ong pane or auomobe rps) ncreases e rsk o deep venous Je w s ). A e re d m mu n y s susp e c e d n a e c e d n d v du a s , romboss (DVT) o e eg vens, as do acors causng ypercoagu- bu ov e r T- c e m mu n o d e c e n c y s n o pre s e n. I m a n e s s aby (e.g., magnancy and nered deecs, suc as acor V Leden; as re d - pu r p e sk n p a qu e s or n o du e s , usu a y on e ow e r see Caper 3). Mae sex and age oder an 50 years aso are assocaed e x re m e s. W me e e s on s m ay n c re a s e n sze and w ncreased rsk. nu mb e r, bu e y usu a y re m a n c on n e d o e sk n an d sub - c u an e ou s ssue. Clncal Features. DVTs produce ew reabe sgns or sympoms. Loca Endemc Afrcan KS ypcay occurs n HIV-negave cdren and manesaons ncude edema, redness, sweng, and pan. In some young adus and can oow an ndoen or aggressve course. I cases, pan can be eced by pressure over afeced vens, squeezng oten nvoves ymp nodes. A severe orm, w promnen vscera e ca musces, or orced dorslexon o e oo (Homan sgn). How- nvovemen, occurs n cdren and s vruay aways aa. ever, sympoms oten are absen, especay n bedrdden paens, and Transpantaton-assocated KS occurs n sod-organ ranspan e absence o ndngs does no excude DVT. In many cases, e rs recpens n e seng o T-ce mmunosuppresson. I pursues an manesaon o DVT s a pumonar y embosm (see Caper 3). To aggressve course and oten nvoves e ymp nodes, mucosa, and preven recurren DVT, ancoaguan reamen s gven, wc may vscera. Lesons oten regress w aenuaon o mmunosuppres- be emporar y or eong, dependng on e eoog y o e DVT. son, bu a e rsk o organ rejecon. AIDS-assocated (epdemc) KS s an AIDS-denng ness and remans e mos common HIV-reaed magnancy wordwde. TUMORS OF BLOOD VESSELS AND LYMPHATICS he ncdence as aen more an 80% n popuaons w access Tumors o bood vesses and ympacs ncude bengn emango- o anrerovra erapy, bu KS s occurs n HIV-neced nd- mas (exremey common), ocay aggressve neopasms a measa- vduas w an ncdence a s 1000-od ger an n e gen- sze nrequeny, and rare, gy magnan angosarcomas. Vascuar era popuaon. AIDS-assocaed KS oten nvoves ymp nodes neopasms may arse rom e endoeum or ces a suppor or and dssemnaes wdey o vscera eary n s course. surround bood vesses. Prmar y umors o arge vesses (aora, pu- monar y arer y, and vena cava) occur nrequeny and are mosy Pathogenes s. KS s an unusua neopasm a key begns as a reac- sarcomas. ve proeraon smuaed by acors produced by HHV-8 neced sroma ces. hese ncude vra omoogs o c yoknes suc as ner- Hemangiomas eukn 6, as we as vra acors a enance ce c yce progresson Hemangiomas are common benign tumors composed of blood- and nerere w e uncon o umor suppressors suc as RB. In lled vessels. e absence o an efecve T-ce response, s proeraon per- Severa varees o emangomas are recognzed, ncudng ypes a sss; w me and cona evouon, may progress o a u-ledged occur preerenay n newborns: magnanc y. 116 CHAPTER 7 Diseases of Blood Vessels Pathogeness. Angosarcomas can arse n e seng o ympedema Morphology. Cu aneous esons progress roug ree s e quen a (e.g., oowng ymp node resecon or breas cancer), radaon, and, s ages: patc, paque, and nodue. Paces are pnk, red, or pur pe rarey, ndweng o oregn bodes (e.g., srapne). Hsorcay, poyv- mac ues comp os ed o daed, r regu ar, and anguae d bo o d ny corde as been assocaed w angosarcoma o e ver. vess es ass o caed w an n rae o cronc nlammaor y ces. Paques (Fg. 7.14A) are ee vaed esons comp os e d o daed der ma vas c uar cannes ned and sur rounded by Morphology. In e skn, angosarcomas rs appear as sma, pump spnde ces. No duar esons are over y neopas c and sarpy demarcaed, red nodues. Advanced esons are arge, lesy con an ncre as ed numb ers o pump, proera ng spnd e ces, red-an o gray-we masses (Fg. 7.15A) w -dened margns oten w nersp ers ed s- ke spaces (Fg. 7.14B). he no duar a bend mpercepby w surroundng srucures. he exen o s age oten s accompaned by no da and vs cera nvovemen, dferenaon s varabe, rangng rom umors a orm vascuar par c uary n e A r can and AIDS-ass o cae d var ans. cannes (Fg. 7.15B) o undferenaed spnde ce umors wou dscernbe bood vesses. Clncal Features. he course o KS vares wdey accordng o e cn- ca seng. Cassc KS s argey resrced o e surace o e body, and surgca resecon usuay s adequae reamen. In KS assocaed Clncal Features. Oder adus are more commony afeced, and esons w mmunosuppresson, resoraon o T-ce uncon by reducng mos oten nvove e skn, sot ssue, breas, and ver. Angosarcomas mmunosuppresson oten s efecve. Smary, or AIDS-assocaed are aggressve umors a nvade ocay and measasze. Compee KS, anrerovra erapy generay s beneca. resecon oten s no possbe, and curren 5-year sur vva raes are ony abou 30%. Angiosarcomas Angosarcoma s a magnan neopasm dened by evdence o endo- ea dferenaon. A B C D Fig. 7.13 Hemangiomas. (A) Hemangioma of the tongue. (B) Histologic appearance in juvenile capillary hemangioma. (C) Pyogenic granuloma of the lip. (D) Histologic appearance in cavernous hemangioma. (A and D, Courtesy John Sexton, MD, Beth Israel Hospital, Boston. B, Courtesy Christopher D.M. Fletcher, MD, Brigham and Women’s Hospital, Boston. C, Courtesy Thomas Rogers, MD, University of Texas Southwestern Medical School, Dallas.) CHAPTER 7 Diseases of Blood Vessels 117 A B Fig. 7.14 Kaposi sarcoma. (A) Characteristic coalescent cutaneous red-purple macules and plaques. (B) Histo- logic view of the nodular stage, demonstrating sheets of plump, proliferating spindle cells and slit-like vascular spaces. (Courtesy Christopher D.M. Fletcher, MD, Brigham and Women’s Hospital, Boston.) A B Fig. 7.15 Angiosarcoma. (A) Angiosarcoma of the right ventricle. (B) Moderately differentiated angiosarcoma with dense clumps of atypical cells lining distinct vascular lumina.