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Scleroderma Long Case                                                                                 Eyes
                                                                                                        Anemia (chronic dz, folate and B12 def, Fe def from chr
                                                                                                        esophagitis, microangiopathic hemolytic anemia)
Chronic disorder characterized by diffuse skin and internal organ fibrosis                              Sjogren’s
Women:men 3:1, symptoms usually appear between 20-40                                                  Mouth
3 forms:                                                                                                Microstomia: open <3cm max
     1. limited cutaneous systemic sclerosis—aka CREST synd
                                                                                 Chest                Roman breastplate tight skin
     2. diffuse cutaneous systemic sclerosis—a/w systemic involvement
                                                                                 Heart                RHF/CCF
     3. morphea (localized scleroderma)—rarely progresses
                                                                                                      Pericardial rub
                                                                                                      Pulmonary HTN
CREST syndrome (limited form)—better prognosis
   Calcinosis                                                                    Lungs                Fibrosis
   Raynaud’s phemenomen                                                                               Effusion
   Esophageal immobility                                                                              Chest infections
   Sclerodactyly                                                                                      Alveolar cell carcinoma
   Telangectasia                                                                 Other joints         Arthropathy
                                                                                                      Flexion deformities
                                                                                 Other                BP, urine dipstick for proteinuria
History
Skin                                        Other organs
       Raynaud’s (90%)                          Polyarthralgia                   Investigations
       Edema                                    Proximal myopathy                  To confirm diagnosis
       Thickened stretched skin                 Fever                              To look for complications
       Cutaneous ulcers                         Dysphagia
       Pigmentation, depigmentation             Lungs                            Bloods         FBC            Anemia
       (vitiligo)                                   SOB (due to anaemia)                        U/E/Cr         Renal failure
                                                Cardiac                                         ANA            Nearly always +ve
Dx criteria—1 major or 2 or more minor              Chest pain - pericarditis                   Scleroderma
•    Major: scleroderma affecting MCP               RHF – edema                                 antibody
     and MTP                                    GI                               Urine          dipstick       Proteinuria
•    Minor: sclerodactyly, digital tip              malabsorption                               urinalysis
     pitting or loss of subst of digital        Renal                            Radio          CXR            Effusion, fibrosis, CA
     finger pads, bibasal pulm fibrosis             Decrease urine - CRF                                       Pericardial effusion, cardiomegaly, CCF
                                                    Frothy urine - proteinuria                  2D echo        RHF
Initial presentation
Investigations done – biopsy etc                                                 Management
Treatment and cx treatment                                                          Supportive, symptomatic
Cx disease
                                                                                 Pt education
                                                                                 Scleroderma Cytotoxics
                                                                                 itself            Early stage: cyclophosphamide, MTX
Physical Exam                                                                                      late stage: penicillamine
General               Cachexia                                                   Raynaud’s       Vasodilators – Ca++ blockers
                      Bird like facies                                           Esophageal      Antacids
Hands                 Raynaud’s                                                  symptoms        PPIs
                      Calcinosis, ulcers                                         HTN             Antihypertensives
                      Telangiectasia
                      Arthropathy                                                Steroids have NO role in scleroderma                                    Digitally signed by DR WANA HLA
                      Contractures                                                                                                                       SHWE
Arms/Skin             Thick tethered skin                                                                                                                DN: cn=DR WANA HLA SHWE,
                      Pigmentation                                                                                                                       c=MY, o=UCSI University, School of
                                                                                                                                                         Medicine, KT-Campus, Terengganu,
                      Vitiligo                                                                                                                           ou=Internal Medicine Group,
                      Proximal myopathy                                                                                                                  email=wunna.hlashwe@gmail.com
                                                                                                                                                         Reason: This document is for UCSI
Head                  Alopecia                                                                                                                           year 4 students.
                                                                                                                                                         Date: 2009.02.22 15:19:28 +08'00'

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Scleroderma long case summary

  • 1. Scleroderma Long Case Eyes Anemia (chronic dz, folate and B12 def, Fe def from chr esophagitis, microangiopathic hemolytic anemia) Chronic disorder characterized by diffuse skin and internal organ fibrosis Sjogren’s Women:men 3:1, symptoms usually appear between 20-40 Mouth 3 forms: Microstomia: open <3cm max 1. limited cutaneous systemic sclerosis—aka CREST synd Chest Roman breastplate tight skin 2. diffuse cutaneous systemic sclerosis—a/w systemic involvement Heart RHF/CCF 3. morphea (localized scleroderma)—rarely progresses Pericardial rub Pulmonary HTN CREST syndrome (limited form)—better prognosis Calcinosis Lungs Fibrosis Raynaud’s phemenomen Effusion Esophageal immobility Chest infections Sclerodactyly Alveolar cell carcinoma Telangectasia Other joints Arthropathy Flexion deformities Other BP, urine dipstick for proteinuria History Skin Other organs Raynaud’s (90%) Polyarthralgia Investigations Edema Proximal myopathy To confirm diagnosis Thickened stretched skin Fever To look for complications Cutaneous ulcers Dysphagia Pigmentation, depigmentation Lungs Bloods FBC Anemia (vitiligo) SOB (due to anaemia) U/E/Cr Renal failure Cardiac ANA Nearly always +ve Dx criteria—1 major or 2 or more minor Chest pain - pericarditis Scleroderma • Major: scleroderma affecting MCP RHF – edema antibody and MTP GI Urine dipstick Proteinuria • Minor: sclerodactyly, digital tip malabsorption urinalysis pitting or loss of subst of digital Renal Radio CXR Effusion, fibrosis, CA finger pads, bibasal pulm fibrosis Decrease urine - CRF Pericardial effusion, cardiomegaly, CCF Frothy urine - proteinuria 2D echo RHF Initial presentation Investigations done – biopsy etc Management Treatment and cx treatment Supportive, symptomatic Cx disease Pt education Scleroderma Cytotoxics itself Early stage: cyclophosphamide, MTX Physical Exam late stage: penicillamine General Cachexia Raynaud’s Vasodilators – Ca++ blockers Bird like facies Esophageal Antacids Hands Raynaud’s symptoms PPIs Calcinosis, ulcers HTN Antihypertensives Telangiectasia Arthropathy Steroids have NO role in scleroderma Digitally signed by DR WANA HLA Contractures SHWE Arms/Skin Thick tethered skin DN: cn=DR WANA HLA SHWE, Pigmentation c=MY, o=UCSI University, School of Medicine, KT-Campus, Terengganu, Vitiligo ou=Internal Medicine Group, Proximal myopathy email=wunna.hlashwe@gmail.com Reason: This document is for UCSI Head Alopecia year 4 students. Date: 2009.02.22 15:19:28 +08'00'