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1.
Article in English | MEDLINE | ID: mdl-36688881

ABSTRACT

Kaposiform hemangioendothelioma is a locally invasive tumor and we were unable to find any previous reports of multifocal progression. Sirolimus, a mammalian target of rapamycin inhibitor, has been widely used to treat kaposiform hemangioendothelioma. Herein, we report a case of multifocal progressive kaposiform hemangioendothelioma, wherein sirolimus treatment caused severe thrombocytopenia. A 12-year-old East Asian girl presented with indurated dark-purple masses on her back. The patient had received three surgical interventions following the first appearance of the masses in 2012 and subsequent reappearances in 2014 and 2016. Kaposiform hemangioendothelioma was diagnosed based on radiological and pathological findings. Two more masses appeared in the following year. The patient was treated with oral sirolimus (2.5 mg/ m2/day) and developed grade 3 thrombocytopenia 8 days later. The patient was uneventfully relieved 5 days later after the withdrawal of sirolimus and the administration of appropriate medications. This rare case indicated that kaposiform hemangioendothelioma could be progressive with local metastatic characteristics in children. Besides, the severe sirolimus-induced complication highlights the importance of serum drug level monitoring during treatment. Physicians should be extremely cautious while treating kaposiform hemangioendothelioma patients with sirolimus.


Subject(s)
Anemia , Hemangioendothelioma , Kasabach-Merritt Syndrome , Sarcoma, Kaposi , Child , Female , Humans , Anemia/chemically induced , Hemangioendothelioma/diagnosis , Hemangioendothelioma/drug therapy , Kasabach-Merritt Syndrome/diagnosis , Kasabach-Merritt Syndrome/drug therapy , Sarcoma, Kaposi/chemically induced , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/drug therapy , Sirolimus/adverse effects
5.
Dermatol Clin ; 39(1): 83-90, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33228864

ABSTRACT

In resource-limited settings, point-of-care diagnostic devices have the potential to reduce diagnostic delays and improve epidemiologic surveillance of dermatologic conditions. We outline novel-point-of care diagnostics that have recently been developed for dermatologic conditions that primarily affect patients living in resource-limited settings, namely, Kaposi sarcoma, cutaneous leishmaniasis, leprosy, Buruli ulcer, yaws, onchocerciasis, and lymphatic filariasis. All of the technologies described in this article are prototypes, and some have undergone field testing. These devices still require validation in real-world settings and effective pricing to have a major impact on dermatologic care in resource-limited settings.


Subject(s)
Buruli Ulcer/diagnosis , Elephantiasis, Filarial/diagnosis , Leishmaniasis, Cutaneous/diagnosis , Leprosy/diagnosis , Onchocerciasis/diagnosis , Point-of-Care Testing , Sarcoma, Kaposi/diagnosis , Yaws/diagnosis , Equipment Design , Health Resources , Humans , Microbiological Techniques/instrumentation , Microbiological Techniques/methods , Microscopy, Confocal/instrumentation , Molecular Diagnostic Techniques/instrumentation , Molecular Diagnostic Techniques/methods , Nucleic Acid Amplification Techniques
8.
Article in English | MEDLINE | ID: mdl-20228569

ABSTRACT

Kaposi's sarcoma (KS) is a multifocal cutaneous and extra cutaneous vascular proliferative disorder. In India, there are only a few cases of HIV-associated KS in published literature. A 26-year-old married man presented with asymptomatic elevated skin lesions over the face, trunk, both upper limbs and lower limbs with a duration of one-and-a-half months. Cutaneous examination revealed multiple violaceous papules and nodules, on the face (right upper and lower eyelids, upper lip), trunk and proximal part of both limbs. Oral cavity showed erythematous plaques, two in number, on the hard palate. Skin biopsy showed proliferation of thin walled capillaries with formation of slit like spaces, spindle cell proliferation, abundant extravasation of RBCs and moderately dense inflammatory infiltrate in the dermis. Thus a clinical diagnosis of cutaneous KS was confirmed. On testing with ELISA for HIV, the patient was for the first time diagnosed as HIV reactive. Thus KS was the presenting manifestation of HIV disease.


Subject(s)
HIV Infections/diagnosis , Sarcoma, Kaposi/diagnosis , Skin Neoplasms/diagnosis , Adult , Diagnosis, Differential , HIV Infections/complications , Humans , Male , Sarcoma, Kaposi/complications , Skin Neoplasms/complications
9.
Article in English | MEDLINE | ID: mdl-19584466

ABSTRACT

Kaposi's sarcoma (KS) is a multifocal neoplastic proliferation of endothelial cells predominantly involving skin and other organs. HIV-associated Kaposi's sarcoma has been rarely reported from India. A 38-year-old male presented with persistent swelling on the left lower limb for one year along with multiple erythematous to dusky papules and plaques of one and half months duration and swelling and black discoloration of right lower limb for one month. Cutaneous examination revealed numerous skin colored and erythematous papules and plaques distributed on the left lower limb on the anteromedial aspect and verrucous plaque on the left sole. Multiple erythematous, grouped papules were present over the soft palate. Skin biopsy showed numerous slit like spaces dissecting into the collagen of the upper and mid-dermis along with 'promontory sign' suggestive of Kaposi's sarcoma. Patient was found to be HIV-positive by ELISA test.


Subject(s)
HIV Infections/diagnosis , HIV-1 , Sarcoma, Kaposi/diagnosis , Adult , Antiretroviral Therapy, Highly Active , Diagnosis, Differential , HIV Infections/complications , HIV Infections/drug therapy , Humans , India , Male , Sarcoma, Kaposi/complications , Sarcoma, Kaposi/drug therapy
10.
Article in English | MEDLINE | ID: mdl-19439884

ABSTRACT

Epidemic Kaposi's sarcoma is one of the malignant neoplasms, which can develop in HIV-infected patients. Although the prevalence of HIV infection is reported to be high in Asian countries, Kaposi's sarcoma is rarely reported. We report a case of Kaposi's sarcoma involving the skin and oral mucosa along with extensive bilateral lymphedema of lower extremities, treated successfully with paclitaxel and antiretrovirals.


Subject(s)
HIV Infections/diagnosis , HIV Infections/drug therapy , Paclitaxel/therapeutic use , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/drug therapy , Adult , HIV Infections/complications , Humans , Male , Sarcoma, Kaposi/complications
11.
s.l; s.n; 2006. 19 p. ilus, tab.
Non-conventional in English | Sec. Est. Saúde SP, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1241867

ABSTRACT

Skin cancer is less common in persons with skin of color than in light-skinned Caucasians but is often associated with greater morbidity and mortality. Thus, it is crucial that physicians become familiar with skin cancer in persons of color so as to maximize the likelihood of early detection of these tumors. In dark-skinned ethnic groups, squamous cell carcinoma is most common; squamous cell carcinoma and melanoma usually occur on nonsun-exposed sites; and ultraviolet radiation is not an important etiologic factor for skin cancer with the exception of basal cell carcinoma. Races of intermediate pigmentation, such as Hispanics and Asians, share epidemiologic and clinical features of dark-skinned ethnic groups and Caucasians. Skin cancers pose a significant risk in skin of color and clinicians should focus on preventive measures in these groups such as regular skin exams, self-examination, public education, and screening programs. LEARNING OBJECTIVE: At the completion of this learning activity, participants should be familiar with the epidemiology and unique clinical features of skin cancer in skin of color and be aware of strategies to prevent skin cancer in skin of color.


Subject(s)
Humans , Skin Neoplasms/surgery , Skin Neoplasms/complications , Skin Neoplasms/diagnosis , Skin Neoplasms/physiopathology , Skin Neoplasms/genetics , Skin Neoplasms/immunology , Skin Neoplasms/prevention & control , Skin Neoplasms/chemistry , Skin Neoplasms/radiotherapy , Skin Neoplasms/rehabilitation , Skin Neoplasms/therapy , Sarcoma, Kaposi/complications , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/physiopathology , Ultraviolet Rays , Ultraviolet Therapy/instrumentation , Ultraviolet Therapy/methods
12.
s.l; s.n; Nov. 2002. 15 p. ilus, tab.
Non-conventional in English | Sec. Est. Saúde SP, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1239163

ABSTRACT

Kaposi's sarcoma (KS) was described by Moritz Kaposi in 1872 and was known for an entire century as a rare disorder of older men usually of Eastern European, Mediterranean, and/or Jewish origin. In the early 1980s, the prevalence of KS began to increase dramatically and soon became the most common malignancy in patients with AIDS, especially those who were male homosexuals. In 1994, a new human herpesvirus (HHV) was found to be present in almost 100% of KS lesions. This virus was found to be a gammaherpesvirus, closely related to Epstein-Barr virus, and was designated HHV-8. Subsequently, HHV-8 DNA was found in almost all specimens of classic KS, endemic KS, and iatrogenic KS, as well as epidemic KS (ie, AIDS KS). It is now believed that HHV-8 is necessary, but not sufficient, to cause KS and that other factors such as immunosuppression play a major role. The use of highly active antiretroviral therapy (HAART) since 1996 has markedly reduced the prevalence of AIDS KS in western countries, but because 99% of the 40 million patients with AIDS in the world cannot afford HAART, KS is still a very common problem. Primary effusion lymphoma and multicentric Castleman's disease are also thought to be due to HHV-8. Although HHV-8 DNA has been described in a number of other cutaneous disorders, there is little evidence that HHV-8 is of etiologic significance in these diseases. The mechanism by which HHV-8 causes KS, primary effusion lymphoma, and multicentric Castleman's disease is not well understood but is thought to involve a number of molecular events, the study of which should further our understanding of viral oncology. (J Am Acad Dermatol 2002;47:641-55.) Learning objective: At the completion of this learning activity, participants should be familiar with Kaposi's sarcoma and other manifestations of human herpesvirus 8.


Subject(s)
Humans , Seroepidemiologic Studies , Open Reading Frames/physiology , /physiology , Castleman Disease/virology , Herpesviridae Infections/virology , Gene Products, tat/genetics , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/epidemiology , Sarcoma, Kaposi/drug therapy , Sarcoma, Kaposi/virology , Antiretroviral Therapy, Highly Active
13.
Lepr Rev ; 73(1): 64-71, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11969128

ABSTRACT

The acquired immunodeficiency syndrome (AIDS) is the result of a human immunodeficiency virus (HIV) infection damaging the cell-mediated immune system. A wide range of opportunistic infections (OI) and tumours develop; additionally, HIV directly damages some organs. The patterns of opportunistic diseases (OD) are different in different parts of the world, depending on the local prevalence of latent and acquired infections and on the survival of HIV-infected patients. OD patterns change as people migrate. Recently introduced highly active anti-retroviral chemotherapy prevents many of the common OIs, but also introduces a new range of toxic pathological damage. Longer survival permits development of new HIV-related diseases. The pathology of HIV/AIDS is not static but changing.


Subject(s)
AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/epidemiology , Mycobacterium Infections/diagnosis , Mycobacterium Infections/epidemiology , Adult , Child , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/epidemiology , Female , Humans , Incidence , Male , Risk Factors , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/epidemiology , Skin Neoplasms/diagnosis , Skin Neoplasms/epidemiology , Survival Analysis , United Kingdom/epidemiology
14.
s.l; Hospital Joao de Barros Barreto; 1990. 18 p.
Monography in Portuguese | LILACS | ID: lil-93939

ABSTRACT

A autora se propoe a relatar caso clinico ocorrido no Hospital Joao de Barros Barreto, diagnosticado por necropsia compo Sarcoma de Kaposi intestinal em paciente portador de SIDA grupo IV, cuja evolucao com hemorragia intestinal grave culminou com exito letal. Dada a importancia desta neoplasia ao considerarmos sua frequente associacao com SIDA, a autora tambem faz breve revisao bibluiografica do assunto, dando enfase ao Sarcoma de Kaposi intestinal, porem sem maiores aprofundamentos em vista da escassa bibbliografia disponivel sobre o assunto


Subject(s)
Adult , Humans , Male , Acquired Immunodeficiency Syndrome , HIV , Intestines/pathology , Sarcoma, Kaposi/pathology , Doxorubicin/adverse effects , Drug Therapy, Combination , Etoposide/therapeutic use , Interferon Type I/therapeutic use , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/drug therapy , Sarcoma, Kaposi/epidemiology , Sarcoma, Kaposi/radiotherapy , Vinblastine/therapeutic use
15.
Arkh Patol ; 51(9): 72-4, 1989.
Article in Russian | MEDLINE | ID: mdl-2596986

ABSTRACT

The paper describes a case of lepromatous lepra diagnosed from the skin biopsy specimen taken in a 23-year-old male patient. It provides histologic signs that are beneficial for correct diagnosis. Emphasis is placed upon the necessity for staining by the Ziehl-Neelsen method to detect microorganisms in infiltrative and granulomatous skin lesions.


Subject(s)
Leprosy, Lepromatous/pathology , Adult , Biopsy , Diagnostic Errors , Humans , Leprosy, Lepromatous/diagnosis , Male , Sarcoma, Kaposi/diagnosis , Sarcoma, Kaposi/pathology
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