Abstract
A 61-year-old female presented with yellowish waxy papules over the periorbital, perinasal and perioral areas, superimposed with purpura upon friction. She had painless diffuse firm swelling of the scalp associated with hair loss, arthritis, and shoulder pain (Figs. 44.1, 44.2, 44.3, 44.4, and 44.5).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Bibliography
Bookland MJ, Bagley CA, Schwarz J, Burger PC, Brem H. Intracavernous trigeminal ganglion amyloidoma: case report. Neurosurgery. 2007;60(3):E574.
Chang YT, Liu HN, Wang W, et al. A study of cytokeratin profiles in localized cutaneous amyloids. Arch Dermatol Res. 2004;296:83–8.
Dee CH, Missirian RJ, Chernoff IJ. Primary amyloidoma of the spine. A case report and review of the literature. Spine (Phila Pa 1976). 1998;23(4):497–500.
Dember LM. Emerging treatment approaches for the systemic amyloidoses. Kidney Int. 2005;68:1377.
Garcia CA, Abell-Aleff PC, Gamb SI, Miller DV. Ultrastructural analysis of amyloidoma. Ultrastruct Pathol. 2009;33(3):123–7.
Gertz MA, Lacy MQ, Dispenzieri A. Amyloidosis: recognition, confirmation prognosis, therapy. Mayo Clin Proc. 1999;74:490–4.
Giorgadze T, Baloch ZW, Thaler ER, Gupta PK. Unsuspected systemic amyloidosis diagnosed by fine-needle aspiration of the salivary gland: case report. Diagn Cytopathol. 2004;31(1):57–9.
Haridas A, Basu S, King A, Pollock J. Primary isolated amyloidoma of the lumbar spine causing neurological compromise: case report and literature review. Neurosurgery. 2005;57(1):E196.
Kyle RA, Greipp PR. Amyloidosis (AL) Clinical and laboratory features in 229 cases. Mayo Clin Proc. 1983;58(10):665–83.
Labro H, Al-Kadhimi Z, Djmil M, Oghlakian R, Alshekhlee A. Brain amyloidoma with cerebral hemorrhage. J Am Osteopath Assoc. 2009;109(7):372–5.
Lachmann HJ, et al. Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis. N Engl J Med. 2002;346:1786.
Lachmann HJ, et al. Outcome in systemic AL amyloidosis in relation to changes in concentration of circulating free immunoglobulin light chains following chemotherapy. Br J Haematol. 2003;122:78.
Lee DD, Huang CY, Wong CK. Dermatopathologic findings in 20 cases of systemic amyloidosis. Am J Dermatopathol. 1998;20:438–42.
Mathew JM, Rajshekhar V. Primary amyloidoma of the thoracic spine. Br J Neurosurg. 1998;12(5):448–51.
Merlini G, Bellotti V. Molecular mechanisms of amyloidosis. N Engl J Med. 2003;349:583.
Mizuno J, Nakagawa H, Tsuji Y, Yamada T. Primary amyloidoma of the thoracic spine presenting with acute paraplegia. Surg Neurol. 2001;55(6):378–82.
Moles MP, Brousseau M, Rachieru AP, Godon A, Schmidt A, Furber A, Rousselet MC, Hunault-Berger M. Tumor like presentation of primitive amyloidosis: amyloidoma. Rev Med Interne. 2007;28(5):339–42. Epub 2007 Jan 26.
Mullins KJ, Meyers SP, Kazee AM, Powers JM, Maurer PK. Primary solitary amyloidosis of the spine: a case report and review of the literature. Surg Neurol. 1997;48(4):405–8.
Murata H, Kusuzaki K, Hashiguchi S, Ueda H, Hirasawa Y. Bilateral metachronous periosteal tibial amyloid tumors. Skeletal Radiol. 2000;29(6):346–8.
Oruckaptan H, Karli Oğuz K, Işikay I, Ruacan S. Amyloidoma of the temporal bone and upper cervical spine; presentation of a rare clinical entity with a brief literature review. Turk Neurosurg. 2009;19(2):159–62. Review.
Racanelli V, D’Amore FP. Localized AL amyloidosis of the colon and clinical features of intestinal obstruction A case report. Ann Ital Med Int. 1999;14(1):58–60.
Roy A, Roy V. Primary systemic amyloidosis. Early diagnosis and therapy can improve survival rates and quality of life. Postgrad Med. 2006;119(1):93–9.
Sanchorawala V, Skinner M, Quillen K, et al. Long-term outcome of patients with AL amyloidosis treated with high-dose melphalan and stem-cell transplantation. Blood. 2007;110:3561–3.
Schröder R, Deckert M, Linke RP. Novel isolated cerebral AL lambda amyloid angiopathy with widespread subcortical distribution and leukoencephalopathy due to atypical monoclonal plasma cell proliferation, and terminal systemic gammopathy. J Neuropathol Exp Neurol. 2009;68(3):286–99.
Silverstein SR. Primary, systemic amyloidosis and the dermatologist: where classic skin lesions may provide the clue for early diagnosis. Dermatol Online J. 2005;11(1):5.
Skinner M. AL amyloidosis: the last 30 years. Amyloid. 2000;7:13–4.
Tabatabai G, Baehring J, Hochberg FH. Primary amyloidoma of the brain parenchyma. Arch Neurol. 2005;62(3):477–80.
Unal A, Sütlap PN, Kýyýk M. Primary solitary amyloidoma of thoracic spine: a case report and review of the literature. Clin Neurol Neurosurg. 2003;105(3):167–9.
Vella FS, Simone B, Antonao S. Vertebral amyloidoma in a patient with primary systemic amyloidosis. Am J Med. 2001;110(7):594–6.
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer-Verlag London
About this chapter
Cite this chapter
El-Darouti, M.A. (2013). Facial and Flexural Deposits Associated with Scalp Swelling. In: Challenging Cases in Dermatology. Springer, London. https://doi.org/10.1007/978-1-4471-4249-2_44
Download citation
DOI: https://doi.org/10.1007/978-1-4471-4249-2_44
Published:
Publisher Name: Springer, London
Print ISBN: 978-1-4471-4248-5
Online ISBN: 978-1-4471-4249-2
eBook Packages: MedicineMedicine (R0)