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1.
Ann Hematol ; 2024 Apr 25.
Article in English | MEDLINE | ID: mdl-38662204

ABSTRACT

Distinguishing key morphologic features and understanding the pathophysiology of common cutaneous manifestations of hematologic disorders is essential to ensure prompt and appropriate treatment. In fact, classic cutaneous signs may provide the first clue to the diagnosis of an underlying hematologic disease. Disorders of coagulation, vascular abnormalities, or cutaneous infiltration and deposition are responsible for the underlying pathophysiology of cutaneous manifestations in the majority of cases. Hematologists often feel ill-equipped in identifying morphologic changes in the skin. Thus, the purpose of this review is to provide a comprehensive overview of classic cutaneous manifestations and diagnostic considerations of the associated hematologic conditions. Though there is a specific focus on non-malignant disorders, those straddling the spectrum of malignancy are also discussed. In many disease states, the skin may serve as an important marker of an emerging hematologic disorder, so close collaboration and multidisciplinary input remain essential to provide optimal and timely care for these patients.

4.
JAMA Dermatol ; 159(7): 772-777, 2023 07 01.
Article in English | MEDLINE | ID: mdl-37256599

ABSTRACT

Importance: Scoring systems for Stevens-Johnson syndrome and epidermal necrolysis (EN) only estimate patient prognosis and are weighted toward comorbidities and systemic features; morphologic terminology for EN lesions is inconsistent. Objectives: To establish consensus among expert dermatologists on EN terminology, morphologic progression, and most-affected sites, and to build a framework for developing a skin-directed scoring system for EN. Evidence Review: A Delphi consensus using the RAND/UCLA appropriateness criteria was initiated with a core group from the Society of Dermatology Hospitalists to establish agreement on the optimal design for an EN cutaneous scoring instrument, terminology, morphologic traits, and sites of involvement. Findings: In round 1, the 54 participating dermatology hospitalists reached consensus on all 49 statements (30 appropriate, 3 inappropriate, 16 uncertain). In round 2, they agreed on another 15 statements (8 appropriate, 7 uncertain). There was consistent agreement on the need for a skin-specific instrument; on the most-often affected skin sites (head and neck, chest, upper back, ocular mucosa, oral mucosa); and that blanching erythema, dusky erythema, targetoid erythema, vesicles/bullae, desquamation, and erosions comprise the morphologic traits of EN and can be consistently differentiated. Conclusions and Relevance: This consensus exercise confirmed the need for an EN skin-directed scoring system, nomenclature, and differentiation of specific morphologic traits, and identified the sites most affected. It also established a baseline consensus for a standardized EN instrument with consistent terminology.


Subject(s)
Stevens-Johnson Syndrome , Humans , Stevens-Johnson Syndrome/diagnosis , Consensus , Delphi Technique , Skin/pathology , Head , Blister/pathology
5.
Int J Low Extrem Wounds ; 22(2): 418-422, 2023 Jun.
Article in English | MEDLINE | ID: mdl-33913352

ABSTRACT

Ulcers of mixed etiology are diagnostically elusive and challenging to treat, especially when rare conditions are superimposed. Pyoderma gangrenosum (PG) is an autoinflammatory, ulcerative skin disease that is difficult to diagnose. Diagnostic criteria exist but there are no specific clinical tests to identify it. We discuss a case of PG initially diagnosed as venous ulcer in the setting of peripheral artery disease, complicated by superinfection, refractory to standard wound care, multiple surgical debridements, revascularization, negative pressure therapy, and parenteral antibiotics. Findings differentiating PG from other wound etiologies are explored, with the aim of improving clinical recognition of this condition.


Subject(s)
Peripheral Vascular Diseases , Pyoderma Gangrenosum , Varicose Ulcer , Humans , Pyoderma Gangrenosum/diagnosis , Pyoderma Gangrenosum/etiology , Pyoderma Gangrenosum/therapy , Skin , Peripheral Vascular Diseases/complications
6.
Dermatol Online J ; 28(5)2022 Oct 15.
Article in English | MEDLINE | ID: mdl-36809128

ABSTRACT

BACKGROUND: Patients with psychiatric dermatoses may be high users of healthcare, especially emergency services. A dermatology urgent care model may reduce healthcare utilization in this population. OBJECTIVE: To determine whether a dermatology urgent care model can reduce healthcare utilization among patients with psychiatric dermatoses. METHODS: We conducted a retrospective chart review of patients seen in dermatology urgent care at Oregon Health and Science University between 2018 and 2020 with diagnoses of Morgellons disease and neurotic excoriations. Rates of diagnosis-related healthcare visits and emergency department visits were annualized before and during engagement with the dermatology department. Rates were compared using paired t-tests. RESULTS: We found an 88.0% reduction in annual rates of healthcare visits (P<0.001) and 77.0% reduction in emergency room visits (P<0.003). Results were unchanged when controlled for gender identity, diagnosis, and substance use. LIMITATIONS: We could not account for healthcare use not included in electronic health record. CONCLUSION: Urgent care models in dermatology may reduce overuse of healthcare and emergency services among patients with psychiatric dermatoses.


Subject(s)
Dermatology , Skin Diseases , Humans , Male , Female , Retrospective Studies , Gender Identity , Delivery of Health Care , Patient Acceptance of Health Care , Ambulatory Care , Skin Diseases/epidemiology
7.
JAMA Dermatol ; 157(6): 712-715, 2021 Jun 01.
Article in English | MEDLINE | ID: mdl-33950191

ABSTRACT

IMPORTANCE: Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is known to cause multiple end-organ complications in its acute phase, but less is known about the long-term association with patients' mental health and quality of life. OBJECTIVE: To examine the chronic physical and psychological sequelae affecting patients with SJS/TEN. DESIGN, SETTING, AND PARTICIPANTS: A survey study conducted at 11 academic health centers in the US evaluated 121 adults diagnosed with SJS/TEN by inpatient consultive dermatologists between January 1, 2009, and September 30, 2019. INTERVENTIONS: Patients completed a survey that included the following validated questionnaires: Patient Health Questionnaire-9 (PHQ-9), Generalized Anxiety Disorder-7 (GAD-7), Primary Care Post-Traumatic Stress Disorder Screen (PC-PTSD), and the 12-item Short Form Health Survey (SF-12). The survey also included questions created by the study team regarding fear, patient education, and long-term sequelae relevant to SJS/TEN. MAIN OUTCOMES AND MEASURES: Primary outcome measures were the percentage of patients reporting long-term physical sequelae; the percentage of patients with positive results on PHQ-9, GAD-7, and PC-PTSD screening; and the numeric score on the SF-12 (score of 50 defined as average physical and mental well-being). RESULTS: A total of 121 individuals (73 women [60.3%]; mean [SD] age, 52.5 [17.1] years) completed the survey (response rate, 29.2%). The most common long-term physical sequelae reported were cutaneous problems (102 of 121 [84.3%]), ocular problems (72 of 121 [59.5%]), and oral mucosal problems (61 of 120 [50.8%]). A total of 53.3% (64 of 120) of the respondents had results indicating depression on the PHQ-9, 43.3% (52 of 120) showed signs of anxiety on the GAD-7, and 19.5% had results indicating PTSD on the PC-PTSD. The mean (SD) SF-12 Physical Component Summary score was 42.4 (22.8), and the mean Mental Component Summary score was 46.1 (20.9). A total of 28.2% (33 of 117) of the respondents were unable to work, 68.1% (81 of 119) were fearful of taking new medications, and 30.0% (36 of 120) avoided taking prescribed medications for a diagnosed medical condition. CONCLUSIONS AND RELEVANCE: This survey study found that long-term physical sequelae, depression, and anxiety appear to be common in patients with SJS/TEN, with implications for health and well-being. Improved awareness of these complications may assist health professionals in offering medical care, counseling, and support to patients with SJS/TEN.


Subject(s)
Stevens-Johnson Syndrome , Adult , Female , Humans , Middle Aged , Mouth Mucosa , Physical Examination/methods , Quality of Life , Retrospective Studies , Stevens-Johnson Syndrome/drug therapy
8.
J Am Acad Dermatol ; 84(6): 1547-1553, 2021 Jun.
Article in English | MEDLINE | ID: mdl-32389716

ABSTRACT

BACKGROUND: Patient outcomes are improved when dermatologists provide inpatient consultations. Inpatient access to dermatologists is limited, illustrating an opportunity to use teledermatology. Little is known about the ability of dermatologists to accurately diagnose disease and manage inpatients with teledermatology, particularly when using nondermatologist-generated clinical data. METHODS: This prospective study assessed the ability of teledermatology to diagnose disease and manage 41 dermatology consultations from a large urban tertiary care center, using internal medicine referral documentation and photographs. Twenty-seven dermatology hospitalists were surveyed. Interrater agreement was assessed by the κ statistic. RESULTS: There was substantial agreement between in-person and teledermatology assessment of the diagnosis with differential diagnosis (median κ = 0.83), substantial agreement in laboratory evaluation decisions (median κ = 0.67), almost perfect agreement in imaging decisions (median κ = 1.0), and moderate agreement in biopsy decisions (median κ = 0.43). There was almost perfect agreement in treatment (median κ = 1.0), but no agreement in follow-up planning (median κ = 0.0). There was no association between raw photograph quality and the primary plus differential diagnosis or primary diagnosis alone. LIMITATIONS: Selection bias and single-center nature. CONCLUSIONS: Teledermatology may be effective in the inpatient setting, with concordant diagnosis, evaluation, and management decisions.


Subject(s)
Dermatology/methods , Hospitalization , Remote Consultation/methods , Skin Diseases/diagnosis , Adult , Aged , Feasibility Studies , Female , Hospitalists/statistics & numerical data , Humans , Male , Middle Aged , Observer Variation , Photography , Prospective Studies , Skin/diagnostic imaging , Surveys and Questionnaires/statistics & numerical data , Tertiary Care Centers
9.
Dermatol Online J ; 26(1)2020 Jan 15.
Article in English | MEDLINE | ID: mdl-32155028

ABSTRACT

Trigeminal trophic syndrome is an uncommon condition characterized by paresthesia, itch, and self-inflicted wounds following the trigeminal dermatome(s). Similar processes adhering to cervical nerve distributions have been reported, calling into question the specificity of trigeminal trophic syndrome for the trigeminal network. Herein, we report patient with trigeminal trophic syndrome adhering to the C2 dermatome, a previously unreported distribution.


Subject(s)
Facial Dermatoses/pathology , Paresthesia/pathology , Skin Ulcer/etiology , Trigeminal Nerve , Aged, 80 and over , Diagnosis, Differential , Facial Dermatoses/complications , Female , Humans , Paresthesia/complications , Pruritus/pathology , Skin Ulcer/pathology , Syndrome
10.
J Am Acad Dermatol ; 82(5): 1262-1267, 2020 May.
Article in English | MEDLINE | ID: mdl-31972258

ABSTRACT

BACKGROUND: Inpatient dermatology has been shown to improve patient outcomes at a reduced cost. Few hospitals have dermatologists available. Teledermatology may allow dermatologists to assess hospitalized patients remotely. OBJECTIVE: To examine the diagnostic concordance between a hospitalist, dermatologist, and teledermatologist using store-and-forward teledermatology. METHODS: For 100 consecutive patients requiring inpatient dermatology consultation, a survey was conducted by all 3 raters to convey diagnostic impressions and therapeutic recommendations. Complete and partial agreements were assessed using the Cohen kappa statistic. RESULTS: Inpatient dermatology consultation often resulted in a change in diagnosis (50.9%) and a change in systemic therapy (41.5%). Likewise, virtual teledermatology consultation would have resulted in a change in diagnosis (54.7%) and a change in systemic therapy (47.2%) at similar rates. Comparing the dermatologist and teledermatologists, diagnostic complete and partial agreement were 52.8% and 84.9%, respectively. Systemic therapy agreement was 77.4%. Teledermatologists recommended biopsy more often (68.5% vs 43.5%). LIMITATIONS: Small sample size, tertiary academic medical center, single rater for inpatient teledermatology with specific inpatient niche. CONCLUSION: Teledermatologists performed comparably to an in-person dermatologist for the diagnosis and management of hospitalized patients with skin conditions. Teledermatology may be a suitable alternative for delivery of inpatient care if no dermatologist is available.


Subject(s)
Dermatologists/statistics & numerical data , Hospitalists/statistics & numerical data , Remote Consultation/statistics & numerical data , Skin Diseases/diagnosis , Academic Medical Centers/statistics & numerical data , Biopsy/statistics & numerical data , Dermatology/methods , Dermatology/statistics & numerical data , Hospitalization/statistics & numerical data , Humans , Skin/pathology , Skin Diseases/pathology , Skin Diseases/therapy , Tertiary Care Centers/statistics & numerical data
11.
J Dermatolog Treat ; 31(7): 723-726, 2020 Nov.
Article in English | MEDLINE | ID: mdl-30998080

ABSTRACT

Background: Pyoderma gangrenosum (PG) is a neutrophilic disorder which classically presents as chronic, painful ulcers on the lower extremities. There is evidence supporting a potential role for intravenous immunoglobulin (IVIG) as adjuvant therapy for treatment-resistant cases; however, it is unclear which patients will most benefit from this modality of treatment - an especially important consideration given the cost per infusion ($5000-$10,000). Thus, we sought to identify the clinical characteristics of patients with refractory PG lesions who demonstrated complete healing when IVIG was incorporated into the therapeutic plan.Methods: We performed a literature search of PubMed/MEDLINE and Embase using the keywords 'pyoderma gangrenosum' and 'IVIG'. We also added four institutional cases. Descriptive statistics were used to analyze the data. Significance was set at p < .05.Results: We discovered a total of 45 cases. Twenty-three patients with treatment-resistant PG had complete healing, 22 had partial or unhealed PG ulcers. Patients with one ulcer were 4.1 (95% CI: 1.1-18.5) times more likely to achieve complete healing than patients with more than one ulcer, when IVIG was added (p = .041).Conclusion: There is increased efficacy of IVIG as a treatment for patients with a solitary treatment-resistant PG lesion compared to patients with multiple refractory lesions.


Subject(s)
Immunoglobulins, Intravenous/therapeutic use , Pyoderma Gangrenosum/drug therapy , Administration, Intravenous , Aged , Drug Resistance , Drug Therapy, Combination , Female , Glucocorticoids/therapeutic use , Humans , Male , Middle Aged , Retrospective Studies
12.
Int Wound J ; 16(6): 1440-1444, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31475449

ABSTRACT

Accurate and prompt diagnosis of skin ulcers is critical to optimise management; however, studies in hospitalised patients are limited. This retrospective review of dermatologic consultations included 272 inpatients with skin ulcers between July 2015 and July 2018 in four U.S. academic hospitals. The median age was 54 years and 45% were male. In 49.3% of the patients, skin ulcers were considered the primary reason for admission. Ulcers of 62% were chronic and 49.6% were located on the lower extremities. Pyoderma gangrenosum (17.3%), infection (12.5%), and exogenous causes (11.8%) were the leading aetiologies; 12% remained diagnostically inconclusive after consultation. Diagnostic agreements pre-dermatology and post-dermatology consult ranged from 0.104 (n = 77, 95% CI 0.051-0.194) to 0.553 (n = 76, 95% CI 0.440-0.659), indicating poor-modest agreement. This study highlights the diagnostic complexity and relative incidences of skin ulcers in the inpatient setting.


Subject(s)
Skin Ulcer/epidemiology , Skin Ulcer/etiology , Adult , Biopsy/statistics & numerical data , Dermatology , Female , Hospitalization , Hospitals, University , Humans , Male , Middle Aged , Pyoderma Gangrenosum/diagnosis , Pyoderma Gangrenosum/epidemiology , Referral and Consultation , Retrospective Studies , Skin Diseases, Infectious/diagnosis , Skin Diseases, Infectious/epidemiology , United States/epidemiology
13.
Dermatol Clin ; 37(4): 537-544, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31466593

ABSTRACT

It is important to recognize paraneoplastic dermatoses because they allow the practitioner to begin an early, directed workup to detect an underlying malignant neoplasm. In this review, several paraneoplastic dermatoses are outlined using existing data to detail each one's association with underlying malignancy, demographics, prognosis, and treatment considerations.


Subject(s)
Neoplasms/diagnosis , Paraneoplastic Syndromes/diagnosis , Skin Diseases/diagnosis , Dermatology , Dermatomyositis/diagnosis , Dermatomyositis/etiology , Gastrointestinal Neoplasms/complications , Gastrointestinal Neoplasms/diagnosis , Hematologic Neoplasms/complications , Hematologic Neoplasms/diagnosis , Humans , Lung Neoplasms/complications , Lung Neoplasms/diagnosis , Neoplasms/complications , POEMS Syndrome/diagnosis , Paraneoplastic Syndromes/etiology , Skin Diseases/etiology , Sweet Syndrome/diagnosis , Sweet Syndrome/etiology
15.
JAMA Dermatol ; 155(1): 79-84, 2019 01 01.
Article in English | MEDLINE | ID: mdl-30383110

ABSTRACT

Importance: Pyoderma gangrenosum and necrotizing Sweet syndrome are diagnostically challenging variants of neutrophilic dermatosis that can clinically mimic the cutaneous and systemic features of necrotizing fasciitis. Improved characterization of these rare variants is needed, as improper diagnosis may lead to inappropriate or delayed treatment and the potential for morbidity. Objective: To determine the characteristics of necrotizing neutrophilic dermatosis to improve diagnostic accuracy and distinguish from infection. Design, Setting, and Participants: A case series of patients with necrotizing neutrophilic dermatosis treated at 3 academic hospitals (University of California San Francisco, Oregon Health and Science University, and University of Minnesota) from January 1, 2015, to December 31, 2017, was performed along with a literature review of related articles published between January 1, 1980, and December 31, 2017. Data were obtained from medical records as well as Medline and Embase databases. All patients had signs resembling necrotizing infection and had a final diagnosis of pyoderma gangrenosum with systemic features or necrotizing Sweet syndrome. Patients were excluded if a diagnosis other than neutrophilic dermatosis was made, if key clinical information was missing, and if reported in a non-English language. Main Outcomes and Measures: Description of key characteristics of necrotizing neutrophilic dermatosis. Results: Overall, 54 patients with necrotizing neutrophilic dermatosis were included, of which 40 had pyoderma gangrenosum with systemic features and 14 had necrotizing Sweet syndrome. Of the 54 patients, 29 (54%) were male and 25 (46%) were female, with a mean (SD) age of 51 (19) years. Skin lesions commonly occurred on the lower (19 [35%]) and upper (13 [24%]) extremities and developed after a surgical procedure (22 [41%]) or skin trauma (10 [19%]). Shock was reported in 14 patients (26%), and leukemoid reaction was seen in 15 patients (28%). Of the patients with necrotizing neutrophilic dermatosis, 51 (94%) were initially misdiagnosed as necrotizing fasciitis and subsequently received inappropriate treatment. Debridement was performed in 42 patients (78%), with a mean (SD) of 2 (2 [range, 1-12]) debridements per patient. Four amputations (7%) were performed. Forty-nine patients (91%) received antibiotics when necrotizing neutrophilic dermatosis was misdiagnosed as an infection, and 50 patients (93%) received systemic corticosteroids; all patients responded to immunosuppressants. Conclusions and Relevance: A complex spectrum of clinical findings of pyoderma gangrenosum and Sweet syndrome with prominent systemic inflammation exists that defines a new subset of neutrophilic dermatoses, termed necrotizing neutrophilic dermatoses; recognizing the difference between this variant and severe infection may prevent unnecessary surgical procedures and prolonged disease morbidity associated with a misdiagnosis and may expedite appropriate medical management.


Subject(s)
Fasciitis, Necrotizing/diagnosis , Immunosuppressive Agents/therapeutic use , Neutrophils/pathology , Skin/pathology , Sweet Syndrome/diagnosis , Diagnosis, Differential , Fasciitis, Necrotizing/drug therapy , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Sweet Syndrome/drug therapy
16.
Hear Res ; 364: 1-11, 2018 07.
Article in English | MEDLINE | ID: mdl-29754876

ABSTRACT

Permanent hearing loss is often a result of damage to cochlear hair cells, which mammals are unable to regenerate. Non-mammalian vertebrates such as birds replace damaged hair cells and restore hearing function, but mechanisms controlling regeneration are not understood. The secreted protein bone morphogenetic protein 4 (BMP4) regulates inner ear morphogenesis and hair cell development. To investigate mechanisms controlling hair cell regeneration in birds, we examined expression and function of BMP4 in the auditory epithelia (basilar papillae) of chickens of either sex after hair cell destruction by ototoxic antibiotics. In mature basilar papillae, BMP4 mRNA is highly expressed in hair cells, but not in hair cell progenitors (supporting cells). Supporting cells transcribe genes encoding receptors for BMP4 (BMPR1A, BMPR1B, and BMPR2) and effectors of BMP4 signaling (ID transcription factors). Following hair cell destruction, BMP4 transcripts are lost from the sensory epithelium. Using organotypic cultures, we demonstrate that treatments with BMP4 during hair cell destruction prevent supporting cells from upregulating expression of the pro-hair cell transcription factor ATOH1, entering the cell cycle, and fully transdifferentiating into hair cells, but they do not induce cell death. By contrast, noggin, a BMP4 inhibitor, increases numbers of regenerated hair cells. These findings demonstrate that BMP4 antagonizes hair cell regeneration in the chicken basilar papilla, at least in part by preventing accumulation of ATOH1 in hair cell precursors.


Subject(s)
Bone Morphogenetic Protein 4/pharmacology , Cell Proliferation/drug effects , Hair Cells, Auditory/drug effects , Labyrinth Supporting Cells/drug effects , Regeneration/drug effects , Animals , Anti-Bacterial Agents/toxicity , Basic Helix-Loop-Helix Transcription Factors/genetics , Basic Helix-Loop-Helix Transcription Factors/metabolism , Bone Morphogenetic Protein 4/genetics , Bone Morphogenetic Protein 4/metabolism , Bone Morphogenetic Protein Receptors/agonists , Bone Morphogenetic Protein Receptors/genetics , Bone Morphogenetic Protein Receptors/metabolism , Carrier Proteins/pharmacology , Cell Communication/drug effects , Cell Transdifferentiation , Chickens , Female , Gentamicins/toxicity , Hair Cells, Auditory/metabolism , Hair Cells, Auditory/pathology , Labyrinth Supporting Cells/metabolism , Labyrinth Supporting Cells/pathology , Male , Signal Transduction/drug effects , Tissue Culture Techniques
17.
Dermatol Online J ; 24(11)2018 Nov 15.
Article in English | MEDLINE | ID: mdl-30695979

ABSTRACT

Vasculitis can be a primary disorder or a cutaneous manifestation of a viral infection. The present case describes an atypical localized cutaneous varicella-zoster virus infection inducing a small vessel vasculitis in a patient with multisystem sarcoidosis. Additionally, we discuss the differential diagnoses and treatment options. Varicella-Zoster infection occurs more frequently in immunosuppressed populations and can present with uncharacteristic clinical manifestations complicating the diagnosis as in the present case.


Subject(s)
Herpes Zoster/diagnosis , Skin Diseases, Vascular/diagnosis , Skin Diseases, Viral/diagnosis , Vasculitis/diagnosis , Aged , Antiviral Agents/therapeutic use , Herpes Zoster/complications , Herpes Zoster/drug therapy , Herpes Zoster/pathology , Humans , Male , Skin Diseases, Vascular/etiology , Skin Diseases, Vascular/pathology , Skin Diseases, Viral/complications , Skin Diseases, Viral/drug therapy , Skin Diseases, Viral/pathology , Vasculitis/etiology , Vasculitis/pathology
18.
Arch Dermatol Res ; 308(4): 269-72, 2016 May.
Article in English | MEDLINE | ID: mdl-26895534

ABSTRACT

Bullous pemphigoid (BP) is a common autoimmune blistering disorder of the elderly. Several diagnostic modalities are available, including clinical impression, histopathology, direct and indirect immunofluorescence, and enzyme-linked immunosorbent assay (ELISA) detection of pathogenic antibodies. In this study, we aim to examine the utility of the newest test, ELISA, in comparison to the constellation of other tests. We describe our clinical experience in which 170 patients diagnosed with bullous pemphigoid had multiple tests performed. BP180 alone showed a sensitivity of 54 % and specificity of 94 %. The positive predictive value (PPV) is 95 % while the negative predictive value (NPV) is 52 %. BP230 alone yielded a sensitivity of 48 % and specificity of 94 %. The PPV is 94 % and the NPV is 49 %. Using both tests in combination yielded a sensitivity of 66 % and specificity of 89 %. The PPV of at least one of two tests returning positive is 92 % while the NPV of dual negative tests is 58 %. Use of ELISAs for suspected cases of BP are an inadequate standalone test, and are only helpful in making the diagnosis should they return positive. However, they would appear to miss about one-third of cases.


Subject(s)
Autoantigens/analysis , Dystonin/analysis , Enzyme-Linked Immunosorbent Assay/methods , Non-Fibrillar Collagens/analysis , Pemphigoid, Bullous/diagnosis , Autoantibodies/blood , Autoantibodies/immunology , Autoantigens/immunology , Humans , Retrospective Studies , Sensitivity and Specificity , Collagen Type XVII
19.
J Am Acad Dermatol ; 73(6): 1031-9, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26412164

ABSTRACT

BACKGROUND: Animal-type melanoma is a rare subtype of melanoma with heavily pigmented dermal epithelioid and spindled melanocytes. Its classification as a subtype of melanoma versus a borderline melanocytic tumor is debated. OBJECTIVES: Our primary objective was to characterize the demographics, clinical presentation, histopathology, management, and outcomes of patients with animal-type melanoma. METHODS: We performed a systematic review and meta-analysis of the English-language literature on animal-type melanoma. RESULTS: We identified 190 cases of animal-type melanoma. They occurred equally in men and women, with Caucasians (53.7%) most commonly affected. The median Breslow depth was 3.8 mm; ulceration was reported present in 15.8%; and dermal mitoses greater than or equal to 1/mm(2) was reported in 27.4%. The most common initial management was wide local excision with sentinel lymph node biopsy (55.7%). In all, 78 patients underwent sentinel lymph node biopsy with 41.0% positivity rate. A total of 32 patients underwent completion lymph node dissection with 34.4% positivity rate. Locoregional recurrence was reported in 15 patients, recurrence with distant metastases in 6 patients, and death in 5 patients. LIMITATIONS: Data were obtained from small studies with limited follow-up. There is no universally accepted definition of animal-type melanoma. CONCLUSION: Prospective studies with complete staging information and molecular profiling may allow further characterization of this tumor.


Subject(s)
Melanocytes/pathology , Melanoma/classification , Melanoma/pathology , Skin Neoplasms/classification , Skin Neoplasms/pathology , Biopsy, Needle , Female , Humans , Immunohistochemistry , Incidence , Male , Melanoma/epidemiology , Prognosis , Prospective Studies , Rare Diseases , Risk Assessment , Skin Neoplasms/epidemiology
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