An Overview of Lower Limb Lymphoedema and Diabetes

Total Page:16

File Type:pdf, Size:1020Kb

An Overview of Lower Limb Lymphoedema and Diabetes Clinical REVIEW An overview of lower limb lymphoedema and diabetes Caroline McIntosh, Tracy Green The prevalence for individuals diagnosed with lower limb lymphoedema and coexisting diabetes is unknown. However, both conditions cause significant problems that can compromise the viability of the lower limbs. An extensive search of the literature including medical databases (MEDLINE, PubMed and CINAHL), plus hand searching through diabetes journals, podiatry journals and wound care journals, was undertaken to search for published literature relating to diabetes and lymphoedema of the lower limb. Prevalence subcutaneous tissues (Yosipovitch et al, Key words Lymphoedema/chronic oedema are 2007). significant causes of morbidity in the Lymphoedema general population. An epidemiological Obesity is increasingly being Lower limb study completed by Moffatt et al (2003) recognised as a major public health Diabetes aimed to determine the magnitude of the problem. The Department of Health Foot problem and the likely impact on health (DoH) (2008) stated that, ‘obesity resources, employment and patients’ is both a highly complex issue for quality of life. The study, which was carried society and a costly debilitating lifestyle out in a primary care trust in south west disease’. Health survey information for London, identified a crude prevalence England, undertaken in 2006, found ymphoedema is a chronic of chronic oedema of 1.33/1000. This that a quarter of the adult population progressive condition for which increased to 5.4/1000 with age (>65 in England are classified as obese, along Lthere is no cure. Unless it is years) and was higher in women. with almost a fifth of all children under managed effectively, lymphoedema can the age of 16 (DoH, 2008). Obesity is, gradually deteriorate and treatment Risk factors therefore, one of the major public health can become increasingly difficult. Many risk factors for lymphoedema have issues in the developing world and is Lymphoedema and chronic oedema are been identified, including non-accidental known to contribute to an increased risk terms that are often interlinked. injury, such as venepuncture (Cole, of heart disease, some cancers and type 2006) and chronic health problems 2 diabetes mellitus. Harwood and Mortimer (1995) linked to obesity, such as diabetes, define lymphoedema as: ‘The hypertension and cardiovascular disease Diabetes mellitus accumulation of lymph in the interstitial (Soran et al, 2006). Diabetes is an escalating problem in spaces caused by a defect in the lymphatic the UK, which may contribute to an system.’ It is marked by an abnormal Fife et al (2008) reviewed the current increased prevalence of lymphoedema collection of excess tissue proteins, evidence base, including case studies in in time, particularly when linked with oedema, chronic inflammation and fibrosis the absence of controlled trials, and found obesity. There are currently an estimated (Harwood and Mortimer, 1995). that there is increasing clinical evidence to 2.35 million people diagnosed with suggest that morbidly obese patients are diabetes in England (DoH, 2007), while Chronic oedema describes oedema predisposed to secondary lymphoedema it is estimated that a further 800,000 that has been present for more than and that primary lymphoedema can individuals are living with undiagnosed three months (Moffatt et al, 2003). induce adult-onset obesity. However, diabetes (National Institute for Health there is at present limited scientific and Clinical Excellence [NICE], 2004). Dr Caroline McIntosh is a Senior Lecturer at the evidence to determine the mechanisms Department of Podiatry, National University of Ireland, by which these events take place, The prevalence of diabetes is Galway; Tracy Green is a Macmillan Lymphoedema Clinical although it is known that obesity impedes predicted to rise to more than 2.5 Nurse Specialist, Macmillan Unit, The Calderdale Royal lymphatic flow, leading to an accumulation million in England by 2010 (DoH, Hospital, Halifax of protein-rich lymphatic fluid in the 2007). This rise is attributable to both Journal of Lymphoedema, 2009, Vol 4, No 1 49 McIntosh, revised and cut2 C.indd 1 9/4/09 08:33:45 Clinical REVIEW an ageing population and also an Clinical features of lymphoedema obesity with co-existent lymphoedema increasing prevalence of obesity, with that are particularly problematic in the has also proven to be an independent the DoH (2007) figures suggesting that lower limbs include: risk factor for erysipelas (Yosipovitch et approximately 9% of the increased 8 Pitting oedema in the initial stages, al, 2007). prevalence of type 2 diabetes will be progressing to non-pitting tissues as a direct consequence of obesity. It the condition progresses Damstra et al (2008) undertook could, therefore, be postulated that 8 Skin changes, including a small (n=40) study in which the incidence of individuals presenting hyperkeratosis, papillomatosis, lymphoscintigraphy of both legs was with both lymphoedema and diabetes, lymphangiomata, fibrosis (Table 1) performed in patients four months after particularly in obese individuals, will 8 Stemmer’s sign their first acute event of erysipelas. escalate over the next few decades. 8 Skin folds Findings from this small sample 8 Distorted/misshapen limb demonstrated that 79% of the patients An extensive search of the literature, 8 Recurrent cellulitis. experienced sub-clinical lymphatic including medical databases (MEDLINE, dysfunction of both legs, suggesting PubMed and CINAHL), plus a hand Skin changes in the lower limb that lymphatic impairment may be a search of diabetes, podiatry and wound Skin changes secondary to diabetes predisposing factor in erysipelas. However, care journals, revealed that there are mellitus are also common, with while diabetes is a known risk factor currently no published data detailing published data suggesting that as many for erysipelas infection, none of the the prevalence of individuals diagnosed as 30% of all patients with diabetes will participants in the study had previously with both lymphoedema and diabetes. present with skin changes during the had a positive diagnosis for diabetes, thus However, a combination of both course of their disease (Ahmed and limiting the external validity of the study. pathologies in the lower limbs can Goldstein, 2006) (Table 2). compromise the viability of the legs and Fungal infection feet, placing the individual at high risk of The impact of obesity (a common Obesity is thought to increase the risk infection, ulceration and necrosis, and, in precursor to both lymphoedema and of cutaneous fungal infections, such as severe cases, the loss of a limb. diabetes) on the skin has received candidiasis. Individuals with diabetes are minimal attention to date, despite the also known to be at an elevated risk of This article aims to explore the fact that obesity is also associated with fungal skin infection, as hyperglycaemia current evidence-base for diabetes a number of dermatoses, including has a detrimental effect on the immune and lymphoedema and discuss the acanthosis nigricans, keratosis pilaris, system. The skin of individuals with implications of both conditions on the hyperkeratosis and skin striae. lymphoedema and diabetes should be lower extremities. It also considers regularly assessed for fungal infection, the appropriate assessment and Furthermore, obesity can heighten particularly in skin folds or between management strategies to aid nurses and the risk of skin breakdown in those digits, where fungi will thrive in the podiatrists in clinical practice. with poor tissue viability, and complicate warm, moist environment. wound management, particularly for Implications of lymphoedema and diabetes those who are morbidly obese (Fife Furthermore, mycologic tests for for the lower limb et al, 2008). In obese patients with the presence of fungal species may Lymphoedema in the diabetic foot lymphoedema, the accumulation of fluid prove beneficial in those individuals is thought to be a combination form in the lower limbs can lead to fibrosis of with ulceration on the legs or feet and of lymphoedema with a complex the skin, decreased oxygen tension and coexisting diabetes and lymphoedema, pathophysiology – microangiopathy leads macrophage function, which provides as fungal infection can be detrimental to to increased permeability of the blood a culture medium for bacterial growth wound healing if left untreated (Missoni capillaries and an increased lymphatic (Yosipovitch et al, 2007). Diabetes is et al, 2006). load. The effects of diabetes can also also known to predispose individuals to affect the blood capillaries of the lymph infection, as the effects of an underlying Specific manifestations of diabetes on nodes, resulting in a general immune vascular disease on the immune system the lower limb deficiency. Lymphatic failure, due to can result in hyperglycaemia and tissue Patients who have lymphoedema, or inflammation following infection, insulin hypoxia (Falanga, 2005). Therefore, are at risk of lymphoedema, also need injections and ulceration, can also result individuals with co-existing lymphoedema to be educated on the effect other (Földi and Földi, 2007). and diabetes are at heightened risk of conditions and treatments may have infection of the lower limbs. on their condition. Diabetes mellitus It is important to identify patients can have a profound impact on the with coexisting lymphoedema/chronic Bacterial infection lower limb – chronic hyperglycaemia oedema and diabetes in
Recommended publications
  • Obesity and Chronic Inflammation in Phlebological and Lymphatic Diseases
    Review 55 Obesity and chronic inflammation in phlebological and lymphatic diseases G. Faerber Centre for Vascular Medicine, Hamburg Keywords increase in intra-abdominal and intertriginous ten mit venösen oder lymphatischen Erkran- Obesity-associated functional venous insuffi- pressure, which in turn leads to an increase in kungen, die gleichzeitig schwer adipös und ciency, obesity-associated lymphoedema, vis- venous pressure in leg vessels, these relation- häufig multimorbide sind, überproportional ceral obesity, chronic inflammation, insulin ships are mainly caused by the metabolic, an. Die Adipositas, vor allem die viszerale, resistance chronic inflammatory and prothrombotic pro- verschlechtert alle Ödemerkrankungen, er- cesses that result from the increase of visceral höht das Risiko für thromboembolische Er- Summary adipose tissue. These processes can be ident- krankungen und postthrombotisches Syn- The prevalence of obesity has continued to ified by low levels of adiponectin and high lev- drom und kann alleinige Ursache sein für die increase considerably during the past 15 els of leptin, insulin, intact proinsulin, PAI-1 Adipositas-assoziierte funktionelle Venenin- years. Particularly noticeable is the marked and proinflammatory cytokines (IL-6, IL-8, suffizienz ohne Nachweis von Obstruktion increase in morbid obesity, which is in turn TNF-α). Therapeutic measures must therefore oder Reflux. Das Adipositas-assoziierte particularly pronounced among the elderly. be aimed primarily at reducing visceral obesity Lymphödem stellt inzwischen den größten Since the prevalence of venous thromboem- and with it hyperinsulinemia or insulin resis- Anteil unter den sekundären Lymphödemen. bolism, chronic venous insufficiency and sec- tance as well as at fighting chronic inflam- Mehr als 50 Prozent der Lipödempatientin- ondary lymphoedema also increases with mation.
    [Show full text]
  • A Case Report of Chronic Sclerosing Panniculitis Hadiuzzaman*, M
    Journal of Pakistan Association of Dermatologists 2010; 20 : 246-248. Case Report A case report of chronic sclerosing panniculitis Hadiuzzaman*, M. Hasibur Rahman*, Nazma Parvin Ansari**, Aminul Islam† *Department of Dermatology, Community Based Medical College, Bangladesh, Mymensingh, Bangladesh. **Department of Pathology, Community Based Medical College, Bangladesh, Mymensingh, Bangladesh †Department of Medicine, Community Based Medical College, Bangladesh, Mymensingh, Bangladesh Abstract Sclerosing panniculitis is a fibrotic process that usually occurs on the legs, commonly in women older than 40. The principal features are indurated woody plaques with erythema, edema, telangiectasia, and hyperpigmentation. Although the exact pathogenesis is uncertain, it is thought to occur as a result of ischemic changes. We present a 28-year-old married female who had a 10- year history of painful sclerotic plaques, repeated ulceration and healing with fibrosis of the both lower legs and abdomen. Venogram and Doppler investigations were normal. Skin biopsy from the edge of the ulcer demonstrated the feature of chronic sclerosing panniculitis. Satisfactory improvement was found with methotrexate 7.5mg weekly for 4 months. No recurrence was noted within 1 year follow up. Key words Sclerosing panniculitis, lipodermatosclerosis. Case report Mild swelling of the legs worse at the end of the day was also reported. Tenderness of the ulcer A 28-year-old married female presented to was worse with dependency. There was no dermatology outpatient, Community Based history of previous trauma to the area, joint Medical College, Bangladesh, with a 10-year complaint, pancreatic disease, or other tender history of painful repeated ulceration and nodular lesions or ulcerations. There was no healing with fibrosis of the both lower legs and significant history of fever and night sweating.
    [Show full text]
  • 2016 Essentials of Dermatopathology Slide Library Handout Book
    2016 Essentials of Dermatopathology Slide Library Handout Book April 8-10, 2016 JW Marriott Houston Downtown Houston, TX USA CASE #01 -- SLIDE #01 Diagnosis: Nodular fasciitis Case Summary: 12 year old male with a rapidly growing temple mass. Present for 4 weeks. Nodular fasciitis is a self-limited pseudosarcomatous proliferation that may cause clinical alarm due to its rapid growth. It is most common in young adults but occurs across a wide age range. This lesion is typically 3-5 cm and composed of bland fibroblasts and myofibroblasts without significant cytologic atypia arranged in a loose storiform pattern with areas of extravasated red blood cells. Mitoses may be numerous, but atypical mitotic figures are absent. Nodular fasciitis is a benign process, and recurrence is very rare (1%). Recent work has shown that the MYH9-USP6 gene fusion is present in approximately 90% of cases, and molecular techniques to show USP6 gene rearrangement may be a helpful ancillary tool in difficult cases or on small biopsy samples. Weiss SW, Goldblum JR. Enzinger and Weiss’s Soft Tissue Tumors, 5th edition. Mosby Elsevier. 2008. Erickson-Johnson MR, Chou MM, Evers BR, Roth CW, Seys AR, Jin L, Ye Y, Lau AW, Wang X, Oliveira AM. Nodular fasciitis: a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest. 2011 Oct;91(10):1427-33. Amary MF, Ye H, Berisha F, Tirabosco R, Presneau N, Flanagan AM. Detection of USP6 gene rearrangement in nodular fasciitis: an important diagnostic tool. Virchows Arch. 2013 Jul;463(1):97-8. CONTRIBUTED BY KAREN FRITCHIE, MD 1 CASE #02 -- SLIDE #02 Diagnosis: Cellular fibrous histiocytoma Case Summary: 12 year old female with wrist mass.
    [Show full text]
  • Panniculitis Martin C
    Panniculitis Martin C. Mihm M.D. Director – Mihm Cutaneous Pathology Consultative Service (MCPCS) Brigham and Women’s Hospital Director – Melanoma Program Brigham and Women’s Hospital and Harvard Medical School Co-Director – Melanoma Program Dana-Farber Cancer Institute and Harvard Medical School Conflicts of Interest • Chairman Scientific Advisory Board – Caliber I.D. Inc. • Member Scientific Advisory Board – MELA Sciences Inc. • Consultant – Novartis • Consultant – Alnylam Disorders of the Subcutis • Septal • Lobular • Mixed • Inflammatory (N/G/L) • Pauci-inflammatory 1 Septal Panniculitis • Erythema nodosum • Necrobiosis lipoidica • Morphea profundus Erythema Nodosum Clinical Features • Young adults • Nodular or plaque like lesions • Anterior aspect of lower legs (common) • Arms or abdomen (occurs occasionally) • Clinical course • Initially erythematous, painful area • Evolves into nodule or plaque • Lasts 10 days to 8 weeks • Fever, malaise, arthralgias (variable s/s) Erythema Nodosum Clinical Features Causation • Systemic diseases: CTD, Behcet’s, Sweet’s, sarcoidosis,etc. • Drugs: Numerous drugs have been associated: penicillin, sulfa, Cipro, isotretinoin, etc. • 30%: idiopathic or of unknown cause.. 2 3 Erythema nodosum : Well Developed Lesion • Septal fibrosis • Septal chronic inflammation • Lymphocytes • Frank Vasculitis may not be present • Granulomatous changes • Small granulomatous aggregates of histiocytes • Miescher’s radial granuloma • Multinucleated giant cells 4 5 6 Erythema nodosum : Morphologic Clues to underlying etiology
    [Show full text]
  • 100 CASES in Dermatology This Page Intentionally Left Blank 100 CASES in Dermatology
    100 CASES in Dermatology This page intentionally left blank 100 CASES in Dermatology Rachael Morris-Jones PhD PCME FRCP Consultant Dermatologist & Honorary Senior Lecturer, King’s College Hospital, London, UK Ann-Marie Powell Consultant Dermatologist, Department of Dermatology, St Thomas’ Hospital, London, UK Emma Benton MB ChB MRCP Post-CCT Clinical Research Fellow, St John’s Institute of Dermatology, Guy’s and St Thomas’ NHS Trust, London, UK 100 Cases Series Editor: Professor P John Rees MD FRCP Dean of Medical Undergraduate Education, King’s College London School of Medicine at Guy’s, King’s and St Thomas’ Hospitals, London, UK First published in Great Britain in 2011 by Hodder Arnold, an imprint of Hodder Education, a division of Hachette UK 338 Euston Road, London NW1 3BH http://www.hodderarnold.com © 2011 Rachael Morris-Jones, Ann-Marie Powell and Emma Benton All rights reserved. Apart from any use permitted under UK copyright law, this publication may only be reproduced, stored or transmitted, in any form, or by any means with prior permission in writing of the publishers or in the case of reprographic production in accordance with the terms of licences issued by the Copyright Licensing Agency. In the United Kingdom such licences are issued by the Copyright Licensing Agency: Saffron House, 6–10 Kirby Street, London EC1N 8TS Hachette UK’s policy is to use papers that are natural, renewable and recyclable products and made from wood grown in sustainable forests. The logging and manufacturing processes are expected to conform to the environmental regulations of the country of origin.
    [Show full text]
  • Consultations in Medical Dermatology Joseph L
    Consultations In Medical Dermatology Joseph L. Jorizzo, MD Professor of Clinical Dermatology Weill Cornell Medical College New York, NY Professor, Founder and Former Chair Department of Dermatology Wake Forest School of Medicine Winston-Salem, NC Conflict of Interest Advisory Boards/Honoraria Amgen Leo Pharmaceuticals Quote from an anonymous patient: “What I am told on the first visit is patient education – on the second an excuse.” Possibilities for a patient who presents with a complex medical dermatosis and systemic signs and symptoms: 1. Clinicopathologic diagnosis of dermatosis integrates all findings eg. Sarcoidosis – skin, eye, lungs, etc 2. Clinicopathologic diagnosis reveals a reactive dermatosis – communication with internist or pediatrician will outline underlying medical conditions eg. Vasculitis 3. No direct relationship – eg. Scabies/Fibromyalgia Patients wishes to know from the internet whether they need x or y therapy for their presumptive diagnosis. Instead it is important to not let the patient “drive” for their own benefit. Step 1. – Clinicopathologic diagnosis- Caution influence of therapy on biopsy and clinical appearance Step 2. – Assess the extent (internal manifestations of disease) Step 3. – Assess for etiology Step 4. - Therapeutic ladder Lichen Planus Key Features • Idiopathic, inflammatory disease of the skin, hair, nails and mucous membranes, seen most commonly in middle-aged adults • Flat-topped violaceous papules and plaques favoring the wrists, forearms, genitalia, distal lower extremities and presacral
    [Show full text]
  • Chronic Venous Insufficiency in Human Immunodeficiency Virus Positive Patients Undergoing Highly Active Antiretroviral Therapy
    Journal of Phlebology and Lymphology Chronic Venous Insufficiency in Human Immunodeficiency Virus- Positive Patients Undergoing Highly Active Antiretroviral Therapy Authors: Marcelo Burihan Calil, MD1, Andre Fonseca Duarte, MD2, Catherine Puliti Hermida Reigada, MD3, Adnan Neser, MD1, Felipe Nasser, MD1, Jose Carlos Ingrund, MD1, Viviane de Almeida Jabur, MD4, Patrícia Carla Piragibe Ramos Burihan, MD4, Gilberto Mitsuo Ukita, PhD2 Adress:1 Santa Marcelina Hospital, 2 University of São Paulo, 3 University of Campinas, 4 University of Santo Amaro E-mail: [email protected] *corresponding author Published: april 2011 Received: 16 November 2011 Journal Phlebology and Lymphology 2011; 4:21-30 Accepted: 12 December 2011 Abstract Introduction: The acquired immunodeficiency syndrome (AIDS) is a chronic and progressive disease with an important worldwide epidemiological impact. Likewise, chronic venous insufficiency (CVI) also represents an extremely relevant pathology. There are no studies correlating both of them. Aim: Characterize human immunodeficiency virus (HIV) positive patients undergoing highly active antiretroviral therapy (HAART) as to the presence of varicose veins and CVI of the lower limbs. Method: A descriptive transversal study. 106 HIV positive patients were evaluated. The majority of the patients were assisted in an infectious disease clinic. The non-parametric test of association qui-square (X2) was used. Results:The time of HIV infection was significant associated with the symptom cramps (P = 0.049). The time of HAART showed a significant association in relation to tingling sensation (P= 0.048). Regarding the time of use of zidovudine, a significant association was observed with tingling sensation (P< 0.01) and edema (P= 0.017). A significant association with referred edema (P= 0.016) was also shown.
    [Show full text]
  • Lipodermatosclerosis: a Commonly Misdiagnosed Complication of Chronic Venous Insufficiency
    Clinical Image TheScientificWorldJOURNAL (2010) 10, 576–577 ISSN 1537-744X; DOI 10.1100/tsw.2010.60 Lipodermatosclerosis: A Commonly Misdiagnosed Complication of Chronic Venous Insufficiency Figure. Lipodermatosclerosis on the left lower leg of a patient suffering from chronic venous insufficiency. Mohammad Kazem Fallahzadeh, Mohammad Khalesi, and Mohammad Reza Namazi* Medicinal and Natural Products Chemistry Research Center and Dermatology Department, Shiraz University of Medical Sciences, Shiraz, Iran E-mail: [email protected] Received February 11, 2010; Revised March 12, 2010; Accepted March 15, 2010; Published April 1, 2010 KEYWORDS: lipodermatosclerosis, venous insufficiency, panniculitis, fibrosis A 50-year-old woman with a history of chronic venous disease presented with erythematous, painful, tense, bound-down plaques on the medial aspects of her lower legs, which were diagnosed as lipodermatosclerosis. *Corresponding author. 576 ©2010 with author. Published by TheScientificWorld; www.thescientificworld.com Fallahzadeh et al.: Lipodermatosclerosis TheScientificWorldJOURNAL (2010) 10, 576–577 Lipodermatosclerosis is a complication of severe chronic venous insufficiency that results from high venous pressure and resulting increased capillary permeability, perivascular fibrin cuffing, and tissue hypoxia. These events culminate in fibrosis and membranous fat necrosis[1]. Lipodermatosclerosis can present as painful, red, indurated plaques that may be easily misdiagnosed as cellulitis, thrombophlebitis, and morphea[2]. It initially develops on the medial aspect of the ankle and then spreads to involve the entire leg circumferentially[3]. In its advanced states, lipodermatosclerosis, along with a lymphedematous upper portion of the leg and an edematous foot, can look like an inverted champagne bottle[3]. Compression therapy, drugs such as stanozolol, and surgical procedures are the current therapeutic options available for this recalcitrant conundrum[2].
    [Show full text]
  • Current Concepts in Dermatology
    CURRENT CONCEPTS IN DERMATOLOGY RICK LIN, D.O., FAOCD PROGRAM CHAIR Faculty Suzanne Sirota Rozenberg, DO, FAOCD Dr. Suzanne Sirota Rozenberg is currently the program director for the Dermatology Residency Training Program at St. John’s Episcopal Hospital in Far Rockaway, NY. She graduated from NYCOM in 1988, did an Internship and Family Practice residency at Peninsula Hospital Center and a residency in Dermatology at St. John’s Episcopal Hospital. She holds Board Certifications from ACOFP, ACOPM – Sclerotherapy and AOCD. Rick Lin, DO, FAOCD Dr. Rick Lin is a board-certified dermatologist practicing in McAllen, TX since 2006. He is the only board-certified Mohs Micrographic Surgeon in the Rio Grande Valley region. Dr. Rick Lin earned his Bachelor degree in Biology at the University of California at Berkeley and received his medical degree from University of North Texas Health Science Center at Fort Worth in 2001. He also graduated with the Master in Public Health Degree at the School of Public Health of the University of North Texas Health Science Center. He then completed a traditional rotating internship at Dallas Southwest Medical Center in 2002. In 2005 he completed his Dermatology residency training at the Northeast Regional Medical Center in Kirksville, Missouri in conjunction with the Dermatology Institute of North Texas. Dr. Rick Lin served as the Chief Resident of the residency training program for two years. He was also the Resident Liaison for the American Osteopathic College of Dermatology for two years prior to the completion of his residency. In addition to general dermatology and dermatopathology, Dr. Lin received specialized training in Mohs Micrographic surgery, advanced aesthetic surgery, and cosmetic dermatology.
    [Show full text]
  • Severity Stratification by Compression Ultrasound Examination in Lipodermatosclerosis and Diabetic Dermopathy Patients: a Report of Three Cases
    CASE SERIES DERMATOLOGY // IMAGING Severity Stratification by Compression Ultrasound Examination in Lipodermatosclerosis and Diabetic Dermopathy Patients: a Report of Three Cases Cristian Podoleanu1, Bogdan Dobrovat2, Simona Stolnicu3,4, Anca Chiriac5,6,7 1 Department of Internal Medicine, University of Medicine and Pharmacy, Tîrgu Mureș, Romania 2 "Gr.T. Popa" University of Medicine and Pharmacy, Iași, Romania 3 Department of Pathology, University of Medicine and Pharmacy, Tîrgu Mureș, Romania 4 Histopat-Invest Laboratory, Tîrgu Mureș, Romania 5 Apollonia University, Department of Dermatology, Iași, Romania 6 “Petru Poni” Institute of Macromolecular Chemistry of the Romanian Academy, Iași, Romania 7 Nicolina Medical Center, Iași, Romania CORRESPONDENCE ABSTRACT Cristian Podoleanu Lipodermatosclerosis and diabetic dermopathy are low-risk skin lesions with many similar Str. Gheorghe Marinescu nr. 38 clinical features, except for venous abnormalities such as chronic venous insufficiency, but 540099 Tîrgu Mureș, Romania are rarely a reason for referring the patient to vascular ultrasound examination. We present 3 Tel: +40 744 573 784 serial cases in which the compression ultrasound examination (CUS) of the venous circulation E-mail: [email protected] of the affected limbs was of utmost importance in the severity stratification. Asymptomatic deep venous thrombosis (DVT) was found in the first two cases, while in the third case the ARTICLE HISTORY CUS excluded any type of vascular involvement, leading to a definite diagnosis of diabetic dermopathy. Lipodermatosclerosis may be associated with asymptomatic DVT due to chronic Received: 19 March, 2017 venous insufficiency, and early referral to CUS positively impacts further patient management. Accepted: 27 May, 2017 Keywords: lipodermatosclerosis, diabetic dermopathy, compression ultrasound, severity strat- ification INTRODUCTION Asymptomatic deep venous thrombosis (DVT) and its related disorder, venous thromboembolism (VTE), are major health care challenges: VTE is the 3rd Bogdan Dobrovat • Str.
    [Show full text]
  • Lipodermatosclerosis
    LIPODERMATOSCLEROSIS http://www.aocd.org Lipodermatosclerosis, also known as sclerosing panniculitis and hypodermitis sclerodermiformis, is an inflammation of the subcutaneous fat, often associated with chronic venous insufficiency. Lipodermatosclerosis is classically found on the inner aspect of the lower extremities above the ankle. It is classified into acute and chronic phases. The acute phase presents clinically as pain, redness, warmth, and tenderness. The chronic, fibrotic phase, presents as red-brown to violet-brown discoloration with firmness and atrophy often appearing as an inverted “champagne bottle.” Lipodermatosclerosis is most commonly found in people with underlying poor circulation in the legs. It is often seen in women over the age of 40 years and men over the age of 70 years. Risk factors include age, immobility, obesity, smoking, family history, and history of deep vein thrombosis or trauma to the venous system. The exact cause is unknown, but evidence suggest that venous hypertension resulting in increased capillary permeability leads to leakage of fibrinogen and white blood cells into the dermis. The fibrinogen forms fibrin cuffs around capillaries, which impedes the exchange of oxygen. This process ultimately causes hypoxia, resulting in venous ulceration. Lipodermatosclerosis is often misdiagnosed as cellulitis. Diagnosis of Lipodermatosclerosis can be done clinically as it does not require biopsy. In fact, biopsy is not advised due to the concern for poor wound healing and the likelihood to develop chronic ulcers. Lipodermatosclerosis is best treated with conservative management. This includes leg elevation, compression stockings, lifestyle modifications (increased physical activity and weight loss, smoking cessation). Physical therapy using ultrasound has been reported as helpful.
    [Show full text]
  • Painful Subcutaneous Nodules of the Lower Extremities
    CCOSMETIASE REPOC TRETCHNIQUE Painful Subcutaneous Nodules of the Lower Extremities Michael Kassardjian, MS-IV; Saira B. Momin, DO; James Q. Del Rosso, DO; Narciss Mobini, MD Painful subcutaneous nodules of the lower extremities are dermatologic manifestations that may be associated with multiple underlying etiologies. Various infectious diseases, autoimmune disorders, and physical and chemical agents may precipitate such a clinical presentation. Keeping the differ- ential diagnosis in mind, appropriate medical workup is essential to accurately diagnose and treat underlying disorders. ainful subcutaneousCOS nodules of the lower DERM patient reported sometimes having symptoms of pruritus extremities are cutaneous processes that tend along with a burning sensation. The patient had a medi- to be attributed to a variety of underlying cal history of hypothyroidism. medical conditions. Infectious diseases, sar- Physical examination revealed tender, indurated, ery- coidosis, reactions to medications, autoim- thematous to hyperpigmented nodules on the left lower Pmune disorders, and malignanciesDo are someNot examples of extremity Copy with evidence of edema and varicose veins underlying disorders that may simulate such a clinical (Figure 1). a 5-mm punch biopsy specimen revealed presentation. a clearly definable cause may be deter- dermal sclerosis with compact eosinophilic collagen mined by generating a complete differential diagnosis, bundles and slight thickening of subcutaneous septae which is necessary for proper workup and effective man- with sparing of the overlying epidermis (Figure 2a). The agement of potentially serious underlying conditions. subcutaneous tissue exhibited microcyst, lipomembra- nous changes, and evidence of fat necrosis. Blood vessels CASE REPORT were thickened with an area of calcification and mild a 66-year-old white woman presented with pain in the superficial perivascular infiltration of lymphocytes also left lower extremity of 1 years’ duration.
    [Show full text]