Primary amyloidosis history and symptoms
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]Shyam Patel [3] Syed Hassan A. Kazmi BSc, MD [4]
Overview
Overview
In primary amyloidosis, the range of symptoms depends on specific tissues and organs involved. Symptoms can be quite diverse.
History and Symptoms
History and Symptoms
History
Patients with amyloidosis may have a positive history of:[1][2]
Symtoms
Symtoms
Common Symptoms
Common symptoms in patients with primary amyloidosis include:[1][3][4][5][6]
- Anasarca
- Bleeding tendency
- Swelling of lower limbs
- Frothy urine
- Chest pain
- Numbness or tingling
- Early satiety
- Joint pains
Less Common Symptoms
Less common symptoms in patients with primary amyloidosis include:[7][8][9][10]
References
References
- ↑ 1.0 1.1 Mahmood S, Palladini G, Sanchorawala V, Wechalekar A (February 2014). “Update on treatment of light chain amyloidosis”. Haematologica. 99 (2): 209–21. doi:10.3324/haematol.2013.087619. PMC 3912950. PMID 24497558.
- ↑ Cichoż-Lach H, Prozorow-Król B, Swatek J, Skrzydło-Radomańska B, Buk L, Zdunek M, Kowalik A, Słomka M (2014). “Hepatomegaly, weight loss and general malaise – the first manifestations of primary systemic amyloidosis”. Prz Gastroenterol. 9 (1): 57–61. doi:10.5114/pg.2014.40853. PMC 4027848. PMID 24868301.
- ↑ Shin SC, Robinson-Papp J (2012). “Amyloid neuropathies”. Mt. Sinai J. Med. 79 (6): 733–48. doi:10.1002/msj.21352. PMC 3531896. PMID 23239211.
- ↑ Rajkumar SV, Gertz MA, Kyle RA (March 1998). “Prognosis of patients with primary systemic amyloidosis who present with dominant neuropathy”. Am. J. Med. 104 (3): 232–7. doi:10.1016/s0002-9343(98)00037-0. PMID 9552085.
- ↑ Dixit R, Gupta R, Dave L, Prasad N, Sharma S (April 2009). “Clinical profile of patients having pulmonary tuberculosis and renal amyloidosis”. Lung India. 26 (2): 41–5. doi:10.4103/0970-2113.48896. PMC 2860413. PMID 20440393.
- ↑ Morais G, Arruda MM, Bonadia J, Pozzan G (2014). “Cardiac amyloidosis: a challenging diagnosis”. Autops Case Rep. 4 (4): 9–17. doi:10.4322/acr.2014.034. PMC 5443128. PMID 28573124. Vancouver style error: initials (help)
- ↑ Thibault I, Vallières I (May 2011). “Macroglossia due to Systemic Amyloidosis: Is There a Role for Radiotherapy?”. Case Rep Oncol. 4 (2): 392–9. doi:10.1159/000330238. PMC 3177795. PMID 21941488.
- ↑ Yiotakis I, Georgolios A, Charalabopoulos A, Hatzipantelis P, Golias C, Charalabopoulos K, Manolopoulos L (September 2009). “Primary localized laryngeal amyloidosis presenting with hoarseness and dysphagia: a case report”. J Med Case Rep. 3: 9049. doi:10.4076/1752-1947-3-9049. PMC 2767149. PMID 19918287.
- ↑ Rowe K, Pankow J, Nehme F, Salyers W (May 2017). “Gastrointestinal Amyloidosis: Review of the Literature”. Cureus. 9 (5): e1228. doi:10.7759/cureus.1228. PMC 5464793. PMID 28611935.
- ↑ McMahan ZH, Sailors JL, Toto R, Olsen NJ (January 2010). “Systemic amyloidosis presenting as chronic diarrhea in a patient with ankylosing spondylitis”. J Clin Rheumatol. 16 (1): 22–5. doi:10.1097/RHU.0b013e3181c78c1a. PMID 20051751.
Looking for the patient version?
© 2026 MyEClinic – IFTM Institut für Telematik in der Medizin GmbH
