Lymphoplasmacytic lymphoma physical examination: Difference between revisions
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[[File:After therapy.png|thumb|300px|none| One year after therapy. The right [[fundus]] exhibited a roundish, subretinal, pseudovitelliform deposit (a). The deposit displayed uneven hyper-[[autofluorescence]] on a fundus [[autofluorescence]] photograph (c) and an uneven staining in [[fluorescein angiography]] (e). It was associated with [[macular edema]] in an [[OCT]] horizontal scan (g). The left eye fundus exhibited a large retinal serous detachment (b), with the accumulation of hyper-autofluorescent [[lipofuscin]] material in autofluorescence fundus photography (d). [[Fluorescein angiography]] was not contributive (f), but OCT showed the absence of central [[photoreceptors]] (h). [https://openi.nlm.nih.gov/detailedresult.php?img=PMC3433005_cop-0003-0236-g02&query=waldenstrom+macroglobulinaemia&it=xg&req=4&npos=27 Source: Brolly A. et al, Department of Ophthalmology, APHP, Hôpital Lariboisière, University Paris Diderot, Sorbonne Paris Cité, Bourges, France.]]] | [[File:After therapy.png|thumb|300px|none| One year after therapy. The right [[fundus]] exhibited a roundish, subretinal, pseudovitelliform deposit (a). The deposit displayed uneven hyper-[[autofluorescence]] on a fundus [[autofluorescence]] photograph (c) and an uneven staining in [[fluorescein angiography]] (e). It was associated with [[macular edema]] in an [[OCT]] horizontal scan (g). The left eye fundus exhibited a large retinal [[serous]] detachment (b), with the accumulation of hyper-autofluorescent [[lipofuscin]] material in [[autofluorescence]] fundus photography (d). [[Fluorescein angiography]] was not contributive (f), but OCT showed the absence of central [[photoreceptors]] (h). [https://openi.nlm.nih.gov/detailedresult.php?img=PMC3433005_cop-0003-0236-g02&query=waldenstrom+macroglobulinaemia&it=xg&req=4&npos=27 Source: Brolly A. et al, Department of Ophthalmology, APHP, Hôpital Lariboisière, University Paris Diderot, Sorbonne Paris Cité, Bourges, France.]]] | ||
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[[File:Flor angiography gif.gif|thumb|300px|none| [[Fluorescein angiography]]: [[Hyperviscosity syndrome|Hyperviscosity]] syndrome characterized by bilateral retinal venous dilation and [[tortuosity]], retinal [[hemorrhages]] and peripheral microaneurysms.[https://openi.nlm.nih.gov/detailedresult.php?img=PMC3433005_cop-0003-0236-g01&query=waldenstrom+macroglobulinaemia&it=xg&req=4&npos=26 Source: Brolly A. et al, Department of Ophthalmology, APHP, Hôpital Lariboisière, University Paris Diderot, Sorbonne Paris Cité, Bourges, France.]]] | [[File:Flor angiography gif.gif|thumb|300px|none| [[Fluorescein angiography]]: [[Hyperviscosity syndrome|Hyperviscosity]] syndrome characterized by bilateral retinal venous dilation and [[tortuosity]], retinal [[hemorrhages]] and peripheral microaneurysms.[https://openi.nlm.nih.gov/detailedresult.php?img=PMC3433005_cop-0003-0236-g01&query=waldenstrom+macroglobulinaemia&it=xg&req=4&npos=26 Source: Brolly A. et al, Department of Ophthalmology, APHP, Hôpital Lariboisière, University Paris Diderot, Sorbonne Paris Cité, Bourges, France.]]] |
Latest revision as of 14:34, 29 October 2019
Lymphoplasmacytic lymphoma Microchapters |
Differentiating Lymphoplasmacytic Lymphoma from other Diseases |
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Case Studies |
Lymphoplasmacytic lymphoma physical examination On the Web |
American Roentgen Ray Society Images of Lymphoplasmacytic lymphoma physical examination |
Risk calculators and risk factors for Lymphoplasmacytic lymphoma physical examination |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2]
Overview
Patients with lymphoplasmacytic lymphoma usually appear oriented to time, place, and person. Physical examination of patients with lymphoplasmacytic lymphoma is usually remarkable for various findings depending on the degree of tissue infiltration by malignant tumor cells, hyperviscosity syndrome, and accumulation of paraprotein. Common physical exam findings include maculopapular lesions, purpura, petechiae, raynaud's phenomenon, skin ulcers, skin necrosis, cold urticaria, macroglobulinemia cutis, pallor, papilledema, retinopathy, lymphadenopathy, jugular venous distension, pleural effusion, lung rales, pulmonary infiltrates, displaced apical impulse, S3 gallop, hepatosplenomegaly causing abdominal distension, peripheral edema due to congestive heart failure, and distal, symmetric, sensorimotor peripheral neuropathy.
Physical Examination
General Appearance
Patients with lymphoplasmacytic lymphoma are generally well-appearing.[1]
Skin
- Maculopapular lesions, plaques, or nodules[2][3][4]
- Purpura
- Raynaud phenomenon
- Petechiae (if platelet count is low)
- Skin ulcers
- Skin necrosis
- Cold urticaria
- Firm, flesh-colored skin papules and nodules also called macroglobulinemia cutis[3]
] |
HEENT
- Pallor
- Papilledema
- Malignant vitritis[5]
- Congestion/sludging of blood in conjunctival vessels
- Retinitis/retinopathy including dilation, segmentation and tortuosity of retinal vessels, mid-peripheral retinal hemorrhages, serous retinal/macular neurosensory detachment, blurred disc margins and fundal exudates on fundoscopic examination[6][7][8]
- Fundoscopic examination should be performed in all patients with symptoms of hyperviscosity and/or IgM ≥3000 mg/dL
] | |
] | ] |
Neck
Respiratory
- Pleural effusion - in 3-5% of patients[10]
- Rales on auscultation
- Pulmonary infiltrates, nodules, masses[10]
Cardiovascular system
Abdomen
Extremity
- Raynaud phenomenon
- Patients may have peripheral edema if disease is complicated by congestive heart failure
Neuromuscular
References
- ↑ Waldenström's macroglobulinemia. MedlinePlus (2015) https://www.nlm.nih.gov/medlineplus/ency/article/000588.htm Accessed on November 15th, 2015
- ↑ Lin P, Bueso-Ramos C, Wilson CS, Mansoor A, Medeiros LJ (2003). "Waldenstrom macroglobulinemia involving extramedullary sites: morphologic and immunophenotypic findings in 44 patients". Am J Surg Pathol. 27 (8): 1104–13. PMID 12883242.
- ↑ 3.0 3.1 Daoud MS, Lust JA, Kyle RA, Pittelkow MR (1999). "Monoclonal gammopathies and associated skin disorders". J Am Acad Dermatol. 40 (4): 507–35, quiz 536-8. PMID 10188670.
- ↑ Veltman GA, van Veen S, Kluin-Nelemans JC, Bruijn JA, van Es LA (1997). "Renal disease in Waldenström's macroglobulinaemia". Nephrol Dial Transplant. 12 (6): 1256–9. PMID 9198063.
- ↑ Orellana J, Friedman AH (1981). "Ocular manifestations of multiple myeloma, Waldenström's macroglobulinemia and benign monoclonal gammopathy". Surv Ophthalmol. 26 (3): 157–69. PMID 6801795.
- ↑ Pilon AF, Rhee PS, Messner LV (2005). "Bilateral, persistent serous macular detachments with Waldenström's macroglobulinemia". Optom Vis Sci. 82 (7): 573–8. PMID 16044069.
- ↑ Avashia JH, Fath DF (1989). "Bilateral central retinal vein occlusion in Waldenström's macroglobulinemia". J Am Optom Assoc. 60 (9): 657–8. PMID 2507620.
- ↑ Goen TM, Terry JE (1986). "Mid-peripheral hemorrhages secondary to Waldenström's macroglobulinemia". J Am Optom Assoc. 57 (2): 109–12. PMID 3081619.
- ↑ Dimopoulos, Meletios A.; Panayiotidis, Panayiotis; Moulopoulos, Lia A.; Sfikakis, Petros; Dalakas, Marinos (2000). "Waldenström's Macroglobulinemia: Clinical Features, Complications, and Management". Journal of Clinical Oncology. 18 (1): 214–214. doi:10.1200/JCO.2000.18.1.214. ISSN 0732-183X.
- ↑ 10.0 10.1 Fadil A, Taylor DE (1998). "The lung and Waldenström's macroglobulinemia". South Med J. 91 (7): 681–5. PMID 9671845.
- ↑ Coimbra J, Costa AP, Pita F, Rosado P, de Almeida LB (1995). "[Neuropathy in Waldenstrom's macroglobulinemia]". Acta Med Port (in Portuguese). 8 (4): 253–7. PMID 7625222.