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1782           Part XI:  Malignant Lymphoid Diseases                                                                                                            Chapter 108:  Immunoglobulin Light-Chain Amyloidosis             1783




               minimum increase of 300 ng/dL. Finally, liver response is defined as a     29.  von Hutten H, Mihatsch M, Lobeck H, et al: Prevalence and origin of amyloid in kidney
               50 percent reduction in the abnormal alkaline phosphatase value, with   biopsies. Am J Surg Pathol 33(8):1198–1205, 2009.
               progression defined as a 50 percent increase of alkaline phosphatase     30.  Said SM, Sethi S, Valeri AM, et al: Renal amyloidosis: Origin and clinicopathologic
                                                                         correlations of 474 recent cases. Clin J Am Soc Nephrol 8(9):1515–1523, 2013.
               above the lowest recorded value. Currently, consensus criteria to define     31.  Gertz MA, Leung N, Lacy MQ, et al: Clinical outcome of immunoglobulin light chain
               response in soft tissues, the gastrointestinal tract, the tongue, the lung,   amyloidosis affecting the kidney. Nephrol Dial Transplant 24(10):3132–3137, 2009.
               or the peripheral nerve do not exist for AL amyloidosis.    32.  Duda SH, Raible RT, Risler T, et al: [Therapeutic bilateral renal artery embolization in
                                                                         the nephrotic syndrome] [in German]. Dtsch Med Wochenschr 119(3):58–62, 1994.
                                                                        33.  Sher T, Gertz MA: Recent advances in the diagnosis and management of cardiac amy-
               REFERENCES                                               34.  Guan J, Mishra S, Falk RH, Liao R: Current perspectives on cardiac amyloidosis. Am J
                                                                         loidosis. Future Cardiol 10(1):131–146, 2014.
                 1.  Bobon  J: [Professor Paul  Divry 1889–1967]  [in  French].  Acta Neurol Psychiatr Belg   Physiol Heart Circ Physiol 302(3):H544–H552, 2012.
                  67(2):143–148, 1967.                                  35.  Suresh R, Grogan M, Maleszewski JJ, et al: Advanced cardiac amyloidosis associated
                 2.  Steensma DP: “Congo” red: Out of Africa? Arch Pathol Lab Med 125(2):250–252, 2001.  with normal interventricular septal thickness: An uncommon presentation of infiltra-
                 3.  Cohen AS, Calkins E: Electron microscopic observations on a fibrous component in   tive cardiomyopathy. J Am Soc Echocardiogr 27(4):440–447, 2014.
                  amyloid of diverse origins. Nature 183(4669):1202–1203, 1959.    36.  Falk RH: Senile systemic amyloidosis: Are regional differences real or do they reflect
                 4.  Murakami T, Uchino M, Ando M: Genetic abnormalities and pathogenesis of familial   different diagnostic suspicion and use of techniques? Amyloid 19 Suppl 1:68–70, 2012.
                  amyloidotic polyneuropathy. Pathol Int 45(1):1–9, 1995.    37.  Leone O, Longhi S, Quarta CC, et al: New pathological insights into cardiac amyloido-
                 5.  Esplin BL, Gertz MA: Current trends in diagnosis and management of cardiac amyloi-  sis: Implications for non-invasive diagnosis. Amyloid 19(2):99–105, 2012.
                  dosis. Curr Probl Cardiol 38(2):53–96, 2013.          38.  Singh V, Fishman JE, Alfonso CE: Primary systemic amyloidosis presenting as constric-
                 6.  Fernandez-Flores A: A review of amyloid staining: Methods and artifacts. Biotech His-  tive pericarditis. Cardiology 118(4):251–255, 2011.
                  tochem 86(5):293–301, 2011.                           39.  Dubrey S, Pollak A, Skinner M, Falk RH: Atrial thrombi occurring during sinus rhythm
                 7.  Picken MM: Non-light-chain immunoglobulin amyloidosis: Time to expand or refine the   in cardiac amyloidosis: Evidence for atrial electromechanical dissociation. Br Heart J
                  spectrum to include light+heavy chain amyloidosis? Kidney Int 83(3):353–356, 2013.  74(5):541–544, 1995.
                 8.  del Pozo Yauner L, Ortiz E, Sanchez R, et al: Influence of the germline sequence on the     40.  Morin J, Schreiber WE, Lee C: Sudden death due to undiagnosed primary amyloidosis.
                  thermodynamic stability and fibrillogenicity of human lambda 6 light chains. Proteins   J Forensic Sci 58(Suppl 1):S250–S252, 2013.
                  72(2):684–692, 2008.                                  41.  Dubrey SW, Rosser G, Dahdal MT, Gillmore JD: Diagnostic dilemma and sudden death
                 9.  Kourelis TV, Kumar SK, Gertz MA, et al: Coexistent multiple myeloma or increased   outcome: A case of amyloid cardiomyopathy. Clin Med 12(6):596–597, 2012.
                  bone marrow plasma cells define equally high-risk populations in patients with immu-    42.  Dhoble A, Khasnis A, Olomu A, Thakur R: Cardiac amyloidosis treated with an
                  noglobulin light chain amyloidosis. J Clin Oncol 31(34):4319–4324, 2013.  implantable cardioverter defibrillator and subcutaneous array lead system: Report of a
                 10.  Madan S, Dispenzieri A, Lacy MQ, et al: Clinical features and treatment response of   case and literature review. Clin Cardiol 32(8):E63–E65, 2009.
                  light chain (AL) amyloidosis diagnosed in patients with previous diagnosis of multiple     43.  Lin G, Dispenzieri A, Kyle R, et al: Implantable cardioverter defibrillators in patients
                  myeloma. Mayo Clin Proc 85(3):232–238, 2010.           with cardiac amyloidosis. J Cardiovasc Electrophysiol 24(7):793–798, 2013.
                 11.  Kyle RA, Linos A, Beard CM, et al: Incidence and natural history of primary sys-    44.  Mohty D, Damy T, Cosnay P, et al: Cardiac amyloidosis: Updates in diagnosis and man-
                  temic amyloidosis in Olmsted County, Minnesota, 1950 through 1989. Blood 79(7):   agement. Arch Cardiovasc Dis 106(10):528–540, 2013.
                  1817–1822, 1992.                                      45.  Yamashita T, Hamidi Asl K, Yazaki M, Benson MD: A prospective evaluation of the
                 12.  Pardanani  A,  Witzig  TE,  Schroeder  G,  et  al:  Circulating  peripheral  blood  plasma   transthyretin Ile122 allele frequency in an African-American population.  Amyloid
                  cells as a prognostic indicator in patients with primary systemic amyloidosis. Blood   12(2):127–130, 2005.
                  101(3):827–830, 2003.                                 46.  Afolabi I, Hamidi Asl K, Nakamura M, et al: Transthyretin isoleucine-122 mutation in
                 13.  Fonseca R, Ahmann GJ, Jalal SM, et al: Chromosomal abnormalities in systemic amy-  African and American blacks. Amyloid 7(2):121–125, 2000.
                  loidosis. Br J Haematol 103(3):704–710, 1998.         47.  Dispenzieri A, Gertz MA, Kumar SK, et al: High sensitivity cardiac troponin T in
                 14.  Bryce AH, Ketterling RP, Gertz MA, et al: Translocation t(11;14) and survival of   patients with immunoglobulin light chain amyloidosis. Heart 100(5):383–388, 2014.
                  patients with light chain (AL) amyloidosis. Haematologica 94(3):380–386, 2009.    48.  Kumar S, Dispenzieri A, Lacy MQ, et al: Revised prognostic staging system for light
                 15.  Kyle RA, Gertz MA: Primary systemic amyloidosis: Clinical and laboratory features in   chain amyloidosis incorporating cardiac biomarkers and serum free light chain mea-
                  474 cases. Semin Hematol 32(1):45–59, 1995.            surements. J Clin Oncol 30(9):989–995, 2012.
                 16.  Lesser BA, Leeper KV Jr, Conway W. Obstructive sleep apnea in amyloidosis treated     49.  Girnius S, Seldin DC, Cibeira MT, Sanchorawala V: New hematologic response crite-
                  with nasal continuous positive airway pressure. Arch Intern Med 148(10):2285–2287,   ria predict survival in patients with immunoglobulin light chain amyloidosis treated
                  1988.                                                  with high-dose melphalan and autologous stem-cell transplantation.  J Clin Oncol
                 17.  Park MA, Mueller PS, Kyle RA, et al: Primary (AL) hepatic amyloidosis: Clinical fea-  31(21):2749–2750, 2013.
                  tures and natural history in 98 patients. Medicine (Baltimore) 82(5):291–298, 2003.    50.  Leung N, Glavey SV, Kumar S, et al: A detailed evaluation of the current renal response
                 18.  Neri A, Rubino P, Macaluso C, Gandolfi SA: Light-chain amyloidosis mimicking giant   criteria in AL amyloidosis: Is it time for a revision? Haematologica 98(6):988–992, 2013.
                  cell arteritis in a bilateral anterior ischemic optic neuropathy case. BMC Ophthalmol     51.  Palladini G, Dispenzieri A, Gertz MA, et al: New criteria for response to treatment in immu-
                  13:82, 2013.                                           noglobulin light chain amyloidosis based on free light chain measurement and cardiac
                 19.  Foli A, Palladini G, Caporali R, et al: The role of minor salivary gland biopsy in the diag-  biomarkers: Impact on survival outcomes. J Clin Oncol 30(36):4541–4549, 2012.
                  nosis of systemic amyloidosis: Results of a prospective study in 62 patients. Amyloid 18     52.  White JA, Kim HW, Shah D, et al: CMR imaging with rapid visual T1 assessment pre-
                  (Suppl 1):80–82, 2011.                                 dicts mortality in patients suspected of cardiac amyloidosis. JACC Cardiovasc Imaging
                 20.  Aljaroudi WA, Desai MY, Tang WH, et al: Role of imaging in the diagnosis and manage-  7(2):143–156, 2014.
                  ment of patients with cardiac amyloidosis: State of the art review and focus on emerging     53.  Mesquita D, Nobre C, Thomas B, et al: Cardiac amyloidosis: Diagnosis using delayed
                  nuclear techniques. J Nucl Cardiol 21(2):271–283, 2014.  enhancement cardiac  magnetic  resonance  imaging  sequences.  Rev Port Cardiol
                 21.  Glaudemans AW, Slart RH, Noordzij W, et al: Utility of 18F-FDG PET(/CT) in patients   32(11):941–945, 2013.
                  with systemic and localized amyloidosis. Eur J Nucl Med Mol Imaging 40(7):1095–1101,     54.  Gerbaud E, Lederlin M, Laurent F: Value of phase-sensitive inversion recovery
                  2013.                                                  sequence to perform and analyse late gadolinium enhancement in cardiac amyloidosis.
                 22.  Hazenberg BP, van Rijswijk MH, Lub-de Hooge MN, et al: Diagnostic performance and   Arch Cardiovasc Dis 102(12):859–860, 2009.
                  prognostic value of extravascular retention of 123I-labeled serum amyloid P compo-    55.  Glaudemans AW, van Rheenen RW, van den Berg MP, et al: Bone scintigraphy with
                  nent in systemic amyloidosis. J Nucl Med 48(6):865–872, 2007.  technetium-hydroxymethylene diphosphonate allows early diagnosis of cardiac
                 23.  Shidham VB, Hunt B, Jardeh SS, et al: Performing and processing FNA of anterior fat   involvement in patients with transthyretin-derived systemic amyloidosis.  Amyloid
                  pad for amyloid. J Vis Exp (44), 2010.                 21(1):35–44, 2014.
                 24.  Linke RP: On typing amyloidosis using immunohistochemistry. Detailed illustrations,     56.  Antoni G, Lubberink M, Estrada S, et al: In vivo visualization of amyloid deposits in the
                  review and a note on mass spectrometry. Prog Histochem Cytochem 47(2):61–132, 2012.  heart with 11C-PIB and PET. J Nucl Med 54(2):213–220, 2013.
                 25.  Schonland SO, Hegenbart U, Bochtler T, et al: Immunohistochemistry in the classifica-    57.  Norero B, Perez-Ayuso RM, Duarte I, et al: Portal hypertension and acute liver failure as
                  tion of systemic forms of amyloidosis: A systematic investigation of 117 patients. Blood   uncommon manifestations of primary amyloidosis. Ann Hepatol 13(1):142–149, 2013.
                  119(2):488–493, 2012.                                 58.  Mousa AY, Abu-Halimah S, Alhalbouni S, et al: Amyloidosis and spontaneous hepatic
                 26.  Sethi S, Vrana JA, Theis JD, et al: Laser microdissection and mass spectrometry-based   bleeding, transcatheter therapy for hepatic parenchymal bleeding with massive intrap-
                  proteomics aids the diagnosis and typing of renal amyloidosis.  Kidney Int 82(2):   eritoneal hemorrhage: A case report and review of the literature.  Vascular 22(5):
                  226–234, 2012.                                         356–360, 2014.
                 27.  Brambilla F, Lavatelli F, Di Silvestre D, et al: Reliable typing of systemic amyloidoses through     59.  Shin SC, Robinson-Papp J. Amyloid neuropathies. Mt Sinai J Med 79(6):733–748, 2012.
                  proteomic analysis of subcutaneous adipose tissue. Blood 119(8):1844–1847, 2012.    60.  Adams D, Lozeron P, Lacroix C: Amyloid neuropathies.  Curr Opin Neurol 25(5):
                 28.  Vrana JA, Gamez JD, Madden BJ, et al: Classification of amyloidosis by laser microdis-  564–572, 2012.
                  section and mass spectrometry-based proteomic analysis in clinical biopsy specimens.     61.  Rajani B, Rajani V, Prayson RA: Peripheral nerve amyloidosis in sural nerve biopsies: A
                  Blood 114(24):4957–4959, 2009.                         clinicopathologic analysis of 13 cases. Arch Pathol Lab Med 124(1):114–118, 2000.






          Kaushansky_chapter 108_p1773-1784.indd   1782                                                                 9/18/15   9:53 AM
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