The mainstay of therapy in lymphangitis is antimicrobial therapy. Supportive therapy includes [[analgesics]], [[anti-inflammatory]] agents, and warm compresses.
The mainstay of therapy in lymphangitis is antimicrobial therapy. Supportive therapy includes [[analgesics]], [[anti-inflammatory]] agents, and warm compresses.
==Medical Therapy <small><small><small><small>'''Adapted from Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases.'''<ref name="Mandell">{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = | pages = }}</ref></small></small></small></small>==
==Medical Therapy==
*Prompt empirical antibiotic therapy that mostly covers [[beta-hemolytic streptococci]] should be started in order to prevent the rapid progression of lymphangitis.
Lymphangitis is typically treated with antimicrobial. More specifically, the treatment regimen differs among the various forms of Lymphangitis:
*[[Staphylococcal]] infection should be suspected if prominent [[suppuration]] is observed at the primary site of infection.
*If the patient does not respond to the initial empirical antibiotic therapy, present with symptoms of systemic toxicity or if the prevalence of [[methicillin-resistant staphylococcus aureus]] ([[MRSA]]) infections is high in the community, empirical coverage should be considered.
*Patients with mild to moderate disease can be managed in an outpatient setting and patients with severe disease should be managed in an inpatient setting.
*While treating the patients with antibiotics, the following should be considered:
**[[Carbapenems]] should not be used in patients with a history of hypersensitivity to [[beta-lactam]]s.
**[[TMP-SMX]] is not recommended for women in the third trimester of [[pregnancy]] and in children under 2 months of age.
**[[Tetracyclines]] should not be used in children under 8 years of age.
*Besides antibiotics, [[analgesics]], [[anti inflammatory medications]], hot and moist compresses can be used to control pain and inflammation.
*The chronic [[Sporotrichosis|sporotrichoid]] form of lymphangitis can be treated with chemotherapy.
*When ''[[Mycobacterium marinum]]'' infection is suspected, confirmation should be assessed utilizing an [[acid-fast bacilli]] analysis and organism isolation.
*Recurrent lymphangitis can lead to chronic [[lymphedema]], which can be treated with leg elevation, intermittent pneumatic compressions, manual massages, and multilayered bandage wrapping.
*Lymphatic [[filariasis]] can be treated with a one-day or a 12-day [[diethylcarbamazine]] regimen. The one-day regimen is as effective as the 12-day regimen.<ref name="cdc.gov">{{Cite web | last = | first = | title = Parasites - Lymphatic Filariasis | url = http://www.cdc.gov/parasites/lymphaticfilariasis/treatment.html | publisher = | date = | accessdate = }}</ref>
==Laboratory Findings of Severe Disease <small><small><small><small>'''Adapted from the 2005 IDSA Practice guidelines for the diagnosis and management of skin and soft-tissue infections.'''<ref name="pmid16231249">{{cite journal| author=Stevens DL, Bisno AL, Chambers HF, Everett ED, Dellinger P, Goldstein EJ et al.| title=Practice guidelines for the diagnosis and management of skin and soft-tissue infections. | journal=Clin Infect Dis | year= 2005 | volume= 41 | issue= 10 | pages= 1373-406 | pmid=16231249 | doi=10.1086/497143 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16231249 }} </ref></small></small></small></small>==
*[[C reactive protein]] over 13 mg/L
*[[CBC]] with marked [[left shift]]
*Elevated [[creatinine]] level
*2 to 3 times the upper level of normal [[creatinine phosphokinase]]
*Low [[bicarbonate]] level
==Signs and Symptoms Suggestive of Severe Infection <small><small><small><small>'''Adapted from the 2005 IDSA Practice guidelines for the diagnosis and management of skin and soft-tissue infections.'''<ref name="pmid16231249">{{cite journal| author=Stevens DL, Bisno AL, Chambers HF, Everett ED, Dellinger P, Goldstein EJ et al.| title=Practice guidelines for the diagnosis and management of skin and soft-tissue infections. | journal=Clin Infect Dis | year= 2005 | volume= 41 | issue= 10 | pages= 1373-406 | pmid=16231249 | doi=10.1086/497143 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16231249 }} </ref></small></small></small></small>==
*[[Hypotension]]
*Cutaneous hemorrhage
*Disproportional pain
*Gas in the tissue
*Skin sloughing
*Violaceous bullae
==Acute Lymphangitis==
==Acute Lymphangitis==
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===Chronic Lymphangitis===
==Chronic Granulomatous Lymphangitis==
====Pathogen Based Therapy====
====Pathogen Based Therapy====
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==Lymphantic Filarisis==
*Lymphatic [[filariasis]] can be treated with a one-day or a 12-day [[diethylcarbamazine]] regimen. The one-day regimen is as effective as the 12-day regimen.<ref name="cdc.gov">{{Cite web | last = | first = | title = Parasites - Lymphatic Filariasis | url = http://www.cdc.gov/parasites/lymphaticfilariasis/treatment.html | publisher = | date = | accessdate = }}</ref>
==Lymphangitic carcinomatosis==
*Currently no effective strategies available in treating lymphangitis carcinomatosa <ref name="pmid22693377">{{cite journal| author=Raja A, Seshadri RA, Sundersingh S| title=Lymphangitis carcinomatosa: report of a case and review of literature. | journal=Indian J Surg Oncol | year= 2010 | volume= 1 | issue= 3 | pages= 274-6 | pmid=22693377 | doi=10.1007/s13193-011-0047-9 | pmc=3244248 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22693377 }} </ref>
*Steroid administration could produce symptomatic improvement mainly by alleviating breathlessness.<ref name="pmid8930034">{{cite journal| author=Bruce DM, Heys SD, Eremin O| title=Lymphangitis carcinomatosa: a literature review. | journal=J R Coll Surg Edinb | year= 1996 | volume= 41 | issue= 1 | pages= 7-13 | pmid=8930034 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8930034 }} </ref>
The mainstay of therapy in lymphangitis is antimicrobial therapy. Supportive therapy includes analgesics, anti-inflammatory agents, and warm compresses.
Medical Therapy
Lymphangitis is typically treated with antimicrobial. More specifically, the treatment regimen differs among the various forms of Lymphangitis:
Empiric Therapy Adapted from Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases.[1]Adapted from Clin Infect Dis. 2005 Nov 15;41(10):1373-406.[2]J Emerg Med. 2013 Jun;44(6):e397-412.[3]Clin Infect Dis. 2011 Feb 1;52(3):e18-55.[4]
▸ Click on the following categories to expand treatment regimens.
▸ Amoxicillin 500 mg PO q8h PLUS ▸ TMP-SMX 1 or 2 double-strength tablets (sulfamethoxazole 800 mg; trimethoprim 160 mg) PO q12h OR ▸ Doxycycline 100 mg PO q12h OR ▸ Minocycline 100 mg PO q12h
For Suspected Methicillin-Resistant Staphylococcus Aureus (MRSA)
▸ Clindamycin 10-13 mg/kg PO q6-8h OR ▸ TMP-SMX 8–12 mg/kg (based on trimethoprim component) PO q12h OR ▸ Doxycycline¶ ≤45 kg: 2 mg/kg PO q12h; >45 kg: 100 mg PO q12h OR ▸ Minocycline 2 mg/kg PO q12h ¶ OR ▸ Linezolid 10 mg/kg PO q8h
¶ Not recommended for children < 8 years of age
For Suspected Beta-Hemolytic Streptococci and Methicillin-Resistant Staphylococcus Aureus (MRSA)
▸ Amoxicillin 500 mg PO q8h PLUS ▸ TMP-SMX 8–12 mg/kg (based on trimethoprim component) PO q12h OR ▸ Doxycycline¶ ≤45 kg: 2 mg/kg PO q12h; >45 kg: 100 mg PO q12h OR ▸ Minocycline¶ 2 mg/kg PO q12h
Pathogen Based Therapy Adapted from Clin Infect Dis. 2005 Nov 15;41(10):1373-406.[2]J Emerg Med. 2013 Jun;44(6):e397-412.[3]Clin Infect Dis. 2011 Feb 1;52(3):e18-55.[4]
▸ Click on the following categories to expand treatment regimens.
▸ Nafcillin 100–150 mg/kg IV q6h OR ▸ Oxacillin 100–150 mg/kg IV q6h OR ▸ Cefazolin 50 mg/kg IV q8h OR ▸ Clindamycin 10–20 mg/kg PO q8h or 25–40 mg/kg IV q8h OR ▸ Erythromycin 10 mg/kg PO q6h OR ▸ Dicloxacillin 25 mg/kg PO q6h OR ▸ Cephalexin 25 mg/kg PO q6h OR ▸ TMP-SMX 8–12 mg/kg (based on trimethoprim component) IV q6h/PO q12h
▸ Vancomycin 30 mg/kg IV q12h OR ▸ Linezolid 600 mg IV/PO q12h OR ▸ Clindamycin 300-450 mg PO q8h or 600 mg/kg IV q8h OR ▸ Daptomycin 4mg/kg IV q24h OR ▸ Doxycycline 100 mg PO q12h OR ▸ Minocycline 100 mg PO q12h OR ▸ TMP-SMX 1 or 2 double-strength tablets (800/160 mg) PO q12h
Children age >28 days
▸ Vancomycin 40 mg/kg IV q6h OR ▸ Linezolid 10 mg/kg IV/PO q12h OR ▸ Clindamycin 10–20 mg/kg PO q8h or 25–40 mg/kg IV q8h OR ▸ TMP-SMX 8–12 mg/kg (based on trimethoprim component) IV q6h/PO q12h
Adapted from Parasites - Lymphatic Filariasis CDC page.[8]
Lymphantic Filarisis
Lymphatic filariasis can be treated with a one-day or a 12-day diethylcarbamazine regimen. The one-day regimen is as effective as the 12-day regimen.[8]
Lymphangitic carcinomatosis
Currently no effective strategies available in treating lymphangitis carcinomatosa [9]
Steroid administration could produce symptomatic improvement mainly by alleviating breathlessness.[10]
↑Mandell, Gerald L.; Bennett, John E. (John Eugene); Dolin, Raphael. (2010). Mandell, Douglas, and Bennett's principles and practice of infectious disease. Philadelphia, PA: Churchill Livingstone/Elsevier.