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1.
Rev Esp Patol ; 57(2): 97-110, 2024.
Article in Spanish | MEDLINE | ID: mdl-38599743

ABSTRACT

This is the second article in a two-part series published in this journal, in which we examine the histopathological characteristics, as well as the differential diagnosis, of the main entities that present as cystic and pseudocystic structures in cutaneous biopsy. In this second article, we address ciliated cutaneous cysts, branchial cysts, Bartholin's cysts, omphalomesenteric cysts, thymic cysts, thyroglossal duct cysts, synovial cysts, and median raphe cysts, as well as mucocele, ganglion, and auricular and digital myxoid pseudocysts.


Subject(s)
Bartholin's Glands , Cysts , Female , Humans , Cysts/pathology , Diagnosis, Differential , Bartholin's Glands/pathology
2.
Rev Esp Patol ; 57(1): 27-41, 2024.
Article in Spanish | MEDLINE | ID: mdl-38246707

ABSTRACT

Cystic structures represent one of the most common findings in dermatopathology. These encompass both cystic tumors and pseudocysts resulting from the accumulation of certain substances, such as mucin. In a two-part series (of which this is the first part), we have reviewed the principal types of cysts and pseudocysts that may be observed in cutaneous biopsies, examining their histopathological features and primary differential diagnoses. This first part encompasses infundibular cysts, eruptive dermoid cysts, pigmented follicular cysts, pilonidal cysts, tricholemmal cysts, milium cysts, hybrid cysts, bronchogenic cysts, as well as steatocystoma, hydrocystoma, and comedones.


Subject(s)
Bronchogenic Cyst , Epidermal Cyst , Humans , Biopsy , Diagnosis, Differential
3.
Pediatr Dermatol ; 37(5): 968-969, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32602176

ABSTRACT

Nilotinib is a new multitargeted tyrosine kinase inhibitor, which is used to treat chronic myelogenous leukemia when intolerance or recurrence to imatinib occurs. We report the case of a 14-year-old patient being treated with nilotinib who developed a keratosis pilaris-like eruption. This cutaneous adverse effect is a rare but increasingly reported side effect of this therapy.


Subject(s)
Abnormalities, Multiple , Darier Disease , Eyebrows/abnormalities , Adolescent , Antineoplastic Agents , Fusion Proteins, bcr-abl , Humans , Protein Kinase Inhibitors/adverse effects , Pyrimidines/adverse effects
5.
Australas J Dermatol ; 60(2): e148-e150, 2019 May.
Article in English | MEDLINE | ID: mdl-30318748

ABSTRACT

High-frequency ultrasonography (HFUS) can help improve dermatofibrosarcoma protuberans (DFSP) recognition. We present three cases of DFSP in which a "jellyfish-like" sonographic pattern was a useful adjunct in formulating the diagnosis. In addition, we review all DFSP ultrasound images available in the literature.


Subject(s)
Dermatofibrosarcoma/diagnostic imaging , Skin Neoplasms/diagnostic imaging , Child , Dermatofibrosarcoma/pathology , Female , Humans , Male , Middle Aged , Skin Neoplasms/pathology , Ultrasonography
7.
Pediatr Dermatol ; 35(5): e276-e280, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29943873

ABSTRACT

High-frequency ultrasonography is a bedside tool increasingly used for the assessment of skin lesions, but there have been few reports about its importance in children with skin signs of hematologic disease. We present three cases to highlight the usefulness of high-frequency ultrasonography in assisting with the diagnosis of these skin lesions.


Subject(s)
Hematologic Neoplasms/pathology , Skin Neoplasms/diagnostic imaging , Ultrasonography/methods , Child , Female , Humans , Infant , Male , Skin/diagnostic imaging , Skin/pathology , Skin Neoplasms/pathology
9.
Indian J Dermatol ; 60(4): 423, 2015.
Article in English | MEDLINE | ID: mdl-26288449

ABSTRACT

Cirsoid aneurysm is a small vascular proliferation characterized by small to medium-sized channels with features of arteries and veins, that present as small, blue or red asymptomatic papule. We report a case of a crisoid aneurysm on the forhead of an HIV patient that suggested a Kaposi sarcoma as a differential diagnosis.

10.
Am J Dermatopathol ; 37(7): 581-4, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25140665

ABSTRACT

Diffuse dermal angiomatosis is a rare benign condition considered a variant of reactive angioendotheliomatosis, usually related to vascular disease such as arteriovenous fistula or severe peripheral vascular disease. The most frequent clinical manifestations range from a solitary erythematous patch to an indurated plaque that may ulcerate. A clinical case of a 60-year-old woman who developed generalized livedoid lesions 2 days after the administration of intravenous trabectedin and subcutaneous pegfilgrastim for a recidivant myxoid liposarcoma has been reported. A biopsy of the skin lesions showed a pronounced proliferation of vessels in the upper dermis that was diagnosed as diffuse dermal angiomatosis.


Subject(s)
Angiomatosis/chemically induced , Drug Eruptions/etiology , Endothelial Cells/drug effects , Skin Diseases, Vascular/chemically induced , Angiomatosis/pathology , Antigens, CD34/analysis , Antineoplastic Agents, Alkylating/adverse effects , Cell Proliferation , Dioxoles/adverse effects , Drug Eruptions/pathology , Endothelial Cells/chemistry , Endothelial Cells/pathology , Female , Filgrastim , Granulocyte Colony-Stimulating Factor/adverse effects , Humans , Middle Aged , Platelet Endothelial Cell Adhesion Molecule-1/analysis , Polyethylene Glycols , Recombinant Proteins/adverse effects , Skin Diseases, Vascular/pathology , Tetrahydroisoquinolines/adverse effects , Trabectedin
11.
Pediatr Dermatol ; 31(3): 406-8, 2014.
Article in English | MEDLINE | ID: mdl-23004681

ABSTRACT

Follicular mucinosis can develop as a primary form or associated with other benign or malignant skin conditions. We present a case of primary follicular mucinosis in which complete clinical remission was achieved after treatment with topical imiquimod 5%. Primary follicular mucinosis (PFM), also called idiopathic alopecia mucinosa, is considered a distinct entity, the clinical course of which is usually benign, but its pathogenesis remains unclear. There is no standard treatment for PFM, and a wide variety of therapies have been described. There are no previous reports of treatment of PFM with imiquimod.


Subject(s)
Adjuvants, Immunologic/administration & dosage , Aminoquinolines/administration & dosage , Mucinosis, Follicular/drug therapy , Mucinosis, Follicular/pathology , Administration, Topical , Biopsy , Child , Humans , Imiquimod , Male , Treatment Outcome
12.
Dermatol Online J ; 19(3): 16, 2013 Mar 15.
Article in English | MEDLINE | ID: mdl-23552013

ABSTRACT

Acral erythema is a frequent cutaneous reaction related to chemotherapy. A patient presented herein developed acral erythema related to cytosine arabinoside treatment and then graft versus host disease (GVHD). Subsequently, worsening of palmar erythema and pain occurred with intravenous cyclosporin infusions.


Subject(s)
Cyclosporine/adverse effects , Cytarabine/therapeutic use , Erythema/chemically induced , Graft vs Host Disease/drug therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Adult , Antineoplastic Agents/therapeutic use , Drug Eruptions/etiology , Erythema/therapy , Humans , Infusions, Intravenous , Male , Methotrexate/therapeutic use
13.
Pediatr Dermatol ; 30(5): e102-3, 2013.
Article in English | MEDLINE | ID: mdl-23406486

ABSTRACT

Circumscribed acral hypokeratosis (CAH) is a rare dermatosis that typically appears as well-dermarcated erythema with a scaly border on the palms or soles of middle-age patients. A pediatric case of CAH has been recently reported in a 10-year-old boy affecting the medial foot since birth. In this report we describe the second congenital case of CAH on the sole.


Subject(s)
Epidermis/pathology , Foot Dermatoses , Keratosis/diagnosis , Keratosis/pathology , Biopsy , Child, Preschool , Diagnosis, Differential , Foot Dermatoses/congenital , Foot Dermatoses/diagnosis , Foot Dermatoses/pathology , Humans , Male
14.
Am J Dermatopathol ; 35(8): e131-4, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23328788

ABSTRACT

Severe combined immunodeficiency includes a group of diseases characterized by different inherited immunological defects. A 4-month-old girl diagnosed with Omenn syndrome, a subtype of severe combined immunodeficiency presenting with generalized erythroderma, was referred to our hospital for an allogeneic stem cell transplantation. Days before transplantation, she developed hyperpigmented macules that increased in number in the following months. As the erythroderma resolved after transplantation, diffuse hypopigmentation was simultaneously noted together with the expansion of hyperpigmented lesions. Cutaneous biopsy samples were taken at different moments, showing features of Omenn syndrome at first, and 2 months later changes consistent with hypopigmentation and repigmentation were observed. Although pigmentary disorders are rarely described in this context, these must be taken into account as a possible alternative diagnosis to graft-versus-host disease and toxicoderma in immunosuppressed patients.


Subject(s)
Pigmentation Disorders/complications , Pigmentation Disorders/pathology , Severe Combined Immunodeficiency/complications , Severe Combined Immunodeficiency/pathology , Female , Humans , Infant , Skin Pigmentation
16.
Int J Dermatol ; 51(6): 722-5, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22607294

ABSTRACT

BACKGROUND: Verrucous carcinoma (VC) of the anogenital area is an uncommon variant of squamous cell carcinoma (SCC). Its treatment is not standardized, but surgical excision must be performed if possible. The traditional approach does not distinguish between conventional SCC and VC, despite the extremely low metastatic potential of VC. Accordingly, most patients reported in the literature have been treated with radical surgery, including regional lymphadenectomy. METHODS: We report two cases in order to describe the oncologic, functional, and esthetic results achieved by Mohs micrographic surgery (MMS) in the treatment of this disease. RESULTS: Good functional and esthetic results were achieved in both patients. No local or nodal relapses were detected during the respective 12- and 27-month follow-ups. CONCLUSIONS: Early recognition of VC and the proper evaluation of deep biopsies will avoid misdiagnosis as SCC and may prevent the occurrence of unnecessary disfiguring interventions. The MMS technique may be considered as a surgical approach in genitoanal VC, although further research is required to confirm this.


Subject(s)
Anus Neoplasms/surgery , Carcinoma, Verrucous/surgery , Mohs Surgery , Perineum/surgery , Skin Neoplasms/surgery , Anus Neoplasms/pathology , Carcinoma, Verrucous/pathology , Esthetics , Female , Humans , Male , Middle Aged , Perineum/pathology , Skin Neoplasms/pathology , Vulvar Lichen Sclerosus/pathology , Vulvar Lichen Sclerosus/surgery
20.
Actas dermo-sifiliogr. (Ed. impr.) ; 93(10): 602-606, dic. 2002. ilus
Article in Es | IBECS | ID: ibc-17018

ABSTRACT

La cirugía oncológica dermatológica en la cara requiere unos conocimientos anatómicos y funcionales amplios y precisos. En la cara se encuentran estructuras con una función perfectamente delimitada, además de un componente estético muy importante. El colgajo de avance con triángulo de descarga o de Burow soluciona defectos de tamaños variables mediante una técnica sencilla con la que se obtienen resultados muy buenos. Las localizaciones ideales para el uso de este colgajo son el labio superior, la región preauricular y la región ciliar lateral. El uso del triángulo de descarga permite cerrar el defecto fácilmente sin tensión y evita la formación de orejas de perro. (AU)


Subject(s)
Aged , Female , Male , Middle Aged , Humans , Surgical Flaps/instrumentation , Surgical Flaps/methods , Surgical Flaps , Surgery, Plastic/methods , Skin Neoplasms/surgery , Skin/surgery , Surgical Procedures, Operative/methods , Surgery, Plastic/standards , Surgery, Plastic/trends
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