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Journal articles on the topic 'Cutaneous tumor'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Sari, Maylita, Lunardi Bintanjoyo, Bagus Haryo Kusumaputra, et al. "A Retrospective Study of Demographic, Clinical, and Histopathological Profiles of Cutaneous Tumors." Berkala Ilmu Kesehatan Kulit dan Kelamin 34, no. 3 (2022): 149–55. http://dx.doi.org/10.20473/bikk.v34.3.2022.149-155.

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Background: In 2007, skin cancers were third most common malignancies in Indonesia. However, profile of cutaneous tumors in our institution has not been studied. Purpose: To evaluate profile of cutaneous tumors in Dermatology and Venerology Outpatient Clinic, Dr. Soetomo General Hospital, Surabaya, Indonesia. Methods: This is a descriptive retrospective study. Inclusion criteria was new cutaneous tumor patients. Exclusion criteria was incomplete data. Medical record and photograph database from 2019-2020 were assessed for demography, clinical features, histopathological examination and final d

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2

RAMÍREZ-BÁRCENA, PATRICIA, MARCO ANTONIO RODRÍGUEZ-CASTELLANOS, DANIEL FAJARDO-BARAJAS, and CECILIA SANDOVAL-TRESS. "Cutaneous Cartilaginous Tumor." Dermatologic Surgery 32, no. 12 (2006): 1513–15. http://dx.doi.org/10.1097/00042728-200612000-00016.

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RAMÍREZ-BÁRCENA, PATRICIA, MARCO ANTONIO RODRÍGUEZ-CASTELLANOS, DANIEL FAJARDO-BARAJAS, and CECILIA SANDOVAL-TRESS. "Cutaneous Cartilaginous Tumor." Dermatologic Surgery 32, no. 12 (2006): 1513–15. http://dx.doi.org/10.1111/j.1524-4725.2006.32365.x.

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4

Romaní, Jorge, Mireia Yébenes, Oscar Escuder, et al. "Cutaneous Desmoid Tumor." Dermatologic Surgery 35, no. 10 (2009): 1582–87. http://dx.doi.org/10.1111/j.1524-4725.2009.01280.x.

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ANDO, KO-ICHI, YOSHINORI GOTO, NORIO HIRABAYASHI, YOSHINARI MATSUMOTO, and MASARU OHASHI. "Cutaneous Cartilaginous Tumor." Dermatologic Surgery 21, no. 4 (1995): 339–41. http://dx.doi.org/10.1111/j.1524-4725.1995.tb00186.x.

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6

Kaye, Valda M., and Louis P. Dehner. "Cutaneous Glomus Tumor." American Journal of Dermatopathology 13, no. 1 (1991): 2–6. http://dx.doi.org/10.1097/00000372-199102000-00002.

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7

Arumugam, Rohini, Leena Dennis Joseph, Vidhya Venkatesan, and C. D. Narayanan. "A rare case of cutaneous granular cell tumour." International Journal of Research in Medical Sciences 9, no. 8 (2021): 2482. http://dx.doi.org/10.18203/2320-6012.ijrms20213104.

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Granular cell tumors are uncommon tumors of uncertain etiology. It accounts for approximately 0.5% of all soft tissue tumors. However, the involvement of skin is rare. Only few cases of cutaneous granular cell tumor is reported till date. Here, we present a case of cutaneous granular cell tumor in a 48 years female patient.

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8

Miller, M. A., A. D. Weaver, P. L. Stogsdill, et al. "Cutaneous Melanocytomas in 10 Young Cattle." Veterinary Pathology 32, no. 5 (1995): 479–84. http://dx.doi.org/10.1177/030098589503200504.

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Ten melanocytomas from 10 cattle were diagnosed by histopathologic examination of biopsy specimens submitted to the Veterinary Medical Diagnostic Laboratory, University of Missouri, between 1 January 1986 and 31 December 1993. One tumor was congenital; the others were first noticed between 2 months and 2 years of age (x = 9.9 months). Six tumors occurred in purebred (3) or crossbred (3) Angus cattle; one tumor each occurred in a Holstein, a Shorthorn, a Simmental, and a beef calf of unrecorded breed or coat color. Five calves were female, and five were male. Five tumors occurred in truncal der

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CORA, Roxana, Adrian Florin GAL, Marian TAULESCU, et al. "Epidemiological Aspects and Differential Diagnosis of the Cutaneous Round Cell Tumors in Dogs." Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Veterinary Medicine 74, no. 1 (2017): 64. http://dx.doi.org/10.15835/buasvmcn-vm:12591.

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Round cell neoplasms (RCNs) are frequent cutaneous lesions in dogs, with high percentages among skin tumors. In this category are included histiocytoma, mast cell tumor, plasmacytoma, lymphoma and transmissible venereal tumor. The aim of the study was to perform an epidemiological study with reference to the cutaneous round cell tumors in a period of 10 years in the Department of Pathology (Faculty of Veterinary Medicine, Cluj-Napoca, Romania). Additionally, in the recorded cases with round cell tumors (mast cell tumor, histiocytoma and lymphoma) we described the main histological and cytologi

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10

Morais, Barbara, Ricardo Iglesio, Carlo Petitto, Fernando Pinto, and Manoel Teixeira. "Cholangiocarcinoma Seeding along a Ventriculoperitoneal Shunt Catheter: A Rare Initial Manifestation." Arquivos Brasileiros de Neurocirurgia: Brazilian Neurosurgery 36, no. 04 (2017): 243–46. http://dx.doi.org/10.1055/s-0037-1607343.

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AbstractCholangiocarcinoma accounts for less than 2% of all malignant neoplasms. Its cutaneous metastases are extremely rare, accounting for 0.0002% of all cases. The ventriculoperitoneal (VP) shunt has been considered a potential route for tumor dissemination. This type of tumor proliferation has been well documented in patients with intra-abdominal metastases secondary to brain tumors and, less frequently, brain metastases secondary to intra-abdominal tumors. In spite of that, there are few reports of cutaneous metastases along the VP shunt catheter trajectory.We present the case of a cholan

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11

Calonje, Eduardo, and Christopher D. M. Fletcher. "Cutaneous Intraneural Glomus Tumor." American Journal of Dermatopathology 17, no. 4 (1995): 395–98. http://dx.doi.org/10.1097/00000372-199508000-00016.

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12

Gianotti, Raffaele, Antonella Coggi, and Elvio Alessi. "Cutaneous Apocrine Mixed Tumor." American Journal of Dermatopathology 20, no. 1 (1998): 53–55. http://dx.doi.org/10.1097/00000372-199802000-00010.

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13

Kudo, Tomoo, Junichi Kamiie, Naoyuki Aihara, et al. "Malignant Leydig cell tumor in dogs: two cases and a review of the literature." Journal of Veterinary Diagnostic Investigation 31, no. 4 (2019): 557–61. http://dx.doi.org/10.1177/1040638719854791.

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Malignant Leydig cell tumor (MLCT) is a rare testicular tumor in dogs. We report herein 2 dogs with MLCT and cutaneous metastasis. Grossly, marked enlargement and distortion of the involved testes were noted; on cut surface, the parenchyma was completely replaced by neoplastic tissue. In addition, these tumors had extensive necrosis and hemorrhage. Case 1 had a rapidly growing cutaneous mass in the left angle of the mouth; the lesion was well-circumscribed and had an indistinct lobular pattern. Case 2 had multiple cutaneous masses in the dorsal neck region, the thoracic back region, and the ri

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14

Sawada, Yu, Emi Mashima, Natsuko Saito-Sasaki, and Motonobu Nakamura. "The Role of Cell Adhesion Molecule 1 (CADM1) in Cutaneous Malignancies." International Journal of Molecular Sciences 21, no. 24 (2020): 9732. http://dx.doi.org/10.3390/ijms21249732.

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Cell adhesion ability is one of the components to establish cell organization and shows a great contribution to human body construction consisting of various types of cells mixture to orchestrate tissue specific function. The cell adhesion molecule 1 (CADM1) is a molecule of cell adhesion with multiple functions and has been identified as a tumor suppressor gene. CADM1 has multifunctions on the pathogenesis of malignancies, and other normal cells such as immune cells. However, little is known about the function of CADM1 on cutaneous cells and cutaneous malignancies. CADM1 plays an important ro

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Nepomnyashchaya, E. M., Yu V. Ulianova, M. A. Engibaryan, T. O. Lapteva, and M. A. Kuznetsova. "Leiomyosarcoma of the scalp and lower leg skin. Clinical cases and literature review." South Russian Journal of Cancer 3, no. 1 (2022): 46–52. http://dx.doi.org/10.37748/2686-9039-2022-3-1-6.

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Malignant soft tissue tumors localized in the skin, particularly leiomyosarcoma, are rare. Cutaneous leiomyosarcomas could have superficial and deep forms, while subcutaneous leiomyosarcomas are usually nodular. The tumor can spread to the underlying muscle fascia. The immunophenotype of leiomyosarcoma is determined by the following antibodies: ASMA, desmin, and N-caldeston; expression of PanCK is also possible. Researchers do not have any common opinion on the clinical course and biological behavior of cutaneous leiomyosarcomas. This is probably due to the tumor heterogeneity and the carcinog

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McAbee, Kevin P., Lori L. Ludwig, Philip J. Bergman, and Shelly J. Newman. "Feline Cutaneous Hemangiosarcoma: A Retrospective Study of 18 Cases (1998–2003)." Journal of the American Animal Hospital Association 41, no. 2 (2005): 110–16. http://dx.doi.org/10.5326/0410110.

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Cutaneous hemangiosarcoma (HSA) has been infrequently reported in dogs and cats. Medical records of 18 cats diagnosed with cutaneous HSA were reviewed. Age at the time of diagnosis, breed, sex, tumor location, tumor size, treatment type, survival time, disease-free interval, and cause of death were evaluated. Aggressive surgical excision of the tumor was attempted in 10 cats. A complete surgical excision was achieved in five of the 10 cats. Median survival times were statistically longer in cats that underwent surgery versus cats that did not. Cats with cutaneous HSA treated with aggressive su

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17

Montazer, Fatemeh, Armaghan Kazeminejad, Ghasem Rahmatpour Rokni, and Sepideh Tayebi. "Case Report: Cutaneous granular cell tumors." F1000Research 7 (July 16, 2018): 1085. http://dx.doi.org/10.12688/f1000research.13015.1.

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Granular cell tumors are uncommon tumors in the deep soft tissue of the extremities, especially those with intramuscular origin, with a good prognosis after surgical resection. We present a case study of a 30 year old man with a skin lesion on his shoulder, which was grown in size over the course of 2 months. Complete tumor excision was done and histopathological findings revealed a marked hyperplasia epidermis with pseudoepitheliomatous pattern. The pathologic report was compatible with a granular cell tumor.

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18

Alici, Omer, Musa Kemal Keles, and Alper Kurt. "A Rare Cutaneous Adnexal Tumor: Malignant Proliferating Trichilemmal Tumor." Case Reports in Medicine 2015 (2015): 1–4. http://dx.doi.org/10.1155/2015/742920.

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Proliferating trichilemmal tumors (PTTs) are neoplasms derived from the outer root sheath of the hair follicle. These tumors, which commonly affect the scalp of elderly women, rarely demonstrate malignant transformation. Although invasion of the tumors into neighboring tissues and being accompanied with anaplasia and necrosis are accepted as findings of malignancy, histological features may not always be sufficient to identify these tumors. The clinical behavior of the tumor may be incompatible with its histological characteristics. Squamous-cell carcinoma should certainly be considered in dif

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19

Lonsdorf, Anke S., Dominic Edelmann, Thomas Albrecht, et al. "Differential Immunoexpression of Inhibitory Immune Checkpoint Molecules and Clinicopathological Correlates in Keratoacanthoma, Primary Cutaneous Squamous Cell Carcinoma and Metastases." Acta Dermato-Venereologica 104 (February 7, 2024): adv13381. http://dx.doi.org/10.2340/actadv.v104.13381.

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Beyond established anti-programmed cell death protein 1/programmed cell death ligand 1 immunotherapy, T-cell immunoreceptor with immunoglobulin and immunoreceptor tyrosine-based inhibition motif domain (TIGIT) and its ligand CD155 are promising novel inhibitory immune checkpoint targets in human malignancies. Yet, in cutaneous squamous cell carcinoma, evidence on the collective expression patterns of these inhibitory immune checkpoints is scarce. Complete tumour sections of 36 cutaneous squamous cell carcinoma, 5 cutaneous metastases and 9 keratoacanthomas, a highly-differentiated, squamoproli

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20

Donizy, Piotr, Joanna P. Wróblewska, Dora Dias-Santagata, et al. "Merkel Cell Carcinoma of Unknown Primary: Immunohistochemical and Molecular Analyses Reveal Distinct UV-Signature/MCPyV-Negative and High Immunogenicity/MCPyV-Positive Profiles." Cancers 13, no. 7 (2021): 1621. http://dx.doi.org/10.3390/cancers13071621.

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Background: Merkel cell carcinomas of unknown primary (MCC-UPs) are defined as deep-seated tumors without an associated cutaneous tumor. Although the distinction has important clinical implications, it remains unclear whether these tumors represent primary tumors of lymph nodes or metastatic cutaneous primaries. Methods: We compared the immunohistochemical profiles of four groups of MCCs (Merkel cell polyomavirus (MCPyV)-positive UP, MCPyV-negative UP, MCPyV-positive known primary (KP), and MCPyV-negative KP) using B-cell and pre-B-cell markers, cell cycle regulating proteins, follicular stem

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21

Paździor-Czapula, K., I. Otrocka-Domagała, T. Rotkiewicz, and M. Gesek. "Cytomorphometry of canine cutaneous histiocytoma." Polish Journal of Veterinary Sciences 17, no. 3 (2014): 413–20. http://dx.doi.org/10.2478/pjvs-2014-0059.

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Abstract A morphometric analysis of tumoral Langerhans cells and activated macrophages was conducted using canine cutaneous tumors (65 cases of canine cutaneous histiocytoma and 7 cases of pyogranuloma). The histiocytic origin of the tumor cells was confirmed using immunohistochemistry. The parameters of the morphometric analysis included cellular and nuclear size and shape and the nuclear: cytoplasmic ratio; the variability of these features was calculated separately for each tumor. The canine cutaneous histiocytoma group was divided into four stages of regression depending on the intensity o

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22

Neta, Michal, Dinaz Naigamwalla, and Dorothee Bienzle. "Perforin Expression in Feline Epitheliotropic Cutaneous Lymphoma." Journal of Veterinary Diagnostic Investigation 20, no. 6 (2008): 831–35. http://dx.doi.org/10.1177/104063870802000623.

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Cutaneous lymphomas are uncommon in people and companion animals. The tumors can be broadly categorized into epitheliotropic and nonepitheliotropic forms, which appear to have different biological behaviors. The present case describes a feline cutaneous epitheliotropic lymphoma. Masses in a 9-year-old cat were first identified on the tail. The cat was treated with chemotherapy, but additional skin masses developed on the flank, face, and ears. Local radiation induced transient tumor regression, but eventual dissemination prompted euthanasia 13 months after initial tumor appearance. Granular ly

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23

Mattos, Kelly Cristina Melgarejo de, Natasha Silva Porto, Juliane Lepper Deleski, Viviana Cauduro Matesco, and Rochelle Gorczak. "Canine cutaneous mastocytoma: case report." Concilium 24, no. 19 (2024): 506–17. http://dx.doi.org/10.53660/clm-4241-24u17.

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Mast cell tumor is a neoplasm with a high incidence in dogs, whose etiopathogenesis and etiology are poorly understood. Originating from the neoplastic proliferation of mast cells, they can be observed in the skin, mainly in the dermis, subcutaneous tissue, or in other organs. The tumors are often solitary, have a varied appearance and size and do not show a predilection for sex, but are observed with a higher incidence in breeds such as Golden Retriever and others. Treatment will depend on the degree of histopathological classification, tumor staging and patient prognosis. The objective of th

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Davies, David R., Kenneth M. Wyatt, John E. Jardine, Ian D. Robertson, and Peter J. Irwin. "Vinblastine and Prednisolone as Adjunctive Therapy for Canine Cutaneous Mast Cell Tumors." Journal of the American Animal Hospital Association 40, no. 2 (2004): 124–30. http://dx.doi.org/10.5326/0400124.

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Twenty-seven dogs with inadequately excised, cutaneous mast cell tumors (MCT; 20 residual microscopic disease, seven marginal excision) were treated with a vinblastine and prednisolone chemotherapeutic protocol. Twenty dogs were available for follow-up examination after 12 months. One dog suffered local recurrence of the tumor, four dogs developed new cutaneous tumors, and one dog had both events. Fourteen dogs were free of MCT. There was no confirmed tumor-related mortality. Although toxicity from the chemotherapy was generally mild, one dog died of sepsis during treatment.

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25

Miedema, Jayson R., and Daniel Zedek. "Cutaneous Meningioma." Archives of Pathology & Laboratory Medicine 136, no. 2 (2012): 208–11. http://dx.doi.org/10.5858/arpa.2010-0505-rs.

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Cutaneous meningioma is a rare tumor that most commonly occurs on the scalp and occurs in both congenital and acquired forms. It invokes a wide clinical differential diagnosis, but diagnosis is based on characteristic histologic and cytologic findings. Congenital lesions can often present years after birth and even in adult patients. Acquired lesions occur in adulthood. We review histologic, cytologic, and electron microscopic findings and explore how these are used to separate this entity from other entities in the differential diagnosis. While ultrastructural and cytologic findings are simil

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Trotter, M. J., R. Colwell, and V. A. Tron. "Thrombospondin-1 and Cutaneous Melanoma." Journal of Cutaneous Medicine and Surgery 7, no. 2 (2003): 136–41. http://dx.doi.org/10.1177/120347540300700208.

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Background: Thrombospondins (TSPs) are recognized as important glycoproteins that regulate a wide variety of cell functions and interactions. TSPs in malignant tumors can both enhance and inhibit tumor progression, invasion, and metastasis, depending on cell type, stromal interactions, and microenvironment. These proteins are potential targets for anticancer therapy. Objective: The aim of our article is to review the role of thrombospondin-1 (TSP1) in cutaneous melanoma. Conclusions: TSP1 expression is variable in melanoma cell lines and tumors. Similar to findings in other human cancers, expr

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27

Molander-McCrary, H., CJ Henry, K. Potter, JW Tyler, and MS Buss. "Cutaneous mast cell tumors in cats: 32 cases (1991-1994)." Journal of the American Animal Hospital Association 34, no. 4 (1998): 281–84. http://dx.doi.org/10.5326/15473317-34-4-281.

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Case records of 32 cats with cutaneous mast cell tumors (CMCTs) were reviewed. Using the Patnaik system for grading canine mast cell tumors, the relationships between histopathological grade and patient survival time and tumor recurrence were examined. Tumor histopathological grade had no prognostic significance. One-, two-, and three-year tumor recurrence rates following surgical excision were 16%, 19%, and 13%, respectively. Incomplete excision was not associated with a higher rate of tumor recurrence.

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Vankipuram, Siddharth, Somil Jaiswal, Manish Jaiswal, and Ankur Bajaj. "Atypically Located Pott’s Puffy Tumor Presenting as Epidural-Cutaneous Fistula." International Journal of Neurology and Neurosurgery 10, no. 2 (2018): 118–20. http://dx.doi.org/10.21088/ijnns.0975.0223.10218.8.

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29

Kim, HJ, EJ Choi, HR Lee, BT Kwon, and SH Do. "Cutaneous extrarenal rhabdoid tumor in a dog: a case report." Veterinární Medicína 60, No. 2 (2016): 115–19. http://dx.doi.org/10.17221/7987-vetmed.

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30

Paudel, Deliya, and Ram Chandra Adhikari. "Cutaneous granular cell tumor: A case report." Journal of Pathology of Nepal 9, no. 1 (2019): 1511–13. http://dx.doi.org/10.3126/jpn.v9i1.23384.

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Granular cell tumor is a rare benign neoplasm of the skin that accounts for 0.5% of all soft-tissue tumors. Granular cell tumor can affect both sexes and in any age, although it is most common in females. The common locations are the head and neck, the tongue is affected in 25% of cases but any internal organs can be affected such as soft tissue, bronchus, stomach, rectum, anus, biliary ducts. Here, we report a 58-year-old female patient who presented with a 4-year history of a slowly growing mass, with a dimension of 5 × 4 cm on her left waist, diagnosed as a Granular cell tumor at histopatho

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Cibull, Thomas L., and Steven D. Billings. "Cutaneous Malignant Ossifying Fibromyxoid Tumor." American Journal of Dermatopathology 29, no. 2 (2007): 156–59. http://dx.doi.org/10.1097/01.dad.0000211530.26047.2b.

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32

Miracco, Clelia, Miranda Raffaelli, Maria Margherita de Santi, Michele Fimiani, and Piero Tosi. "Solitary Cutaneous Reticulum Cell Tumor." American Journal of Dermatopathology 10, no. 1 (1988): 47–53. http://dx.doi.org/10.1097/00000372-198802000-00006.

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33

Tope, Whitney D. "Cutaneous Tumor in a Child." Archives of Dermatology 128, no. 5 (1992): 683. http://dx.doi.org/10.1001/archderm.1992.01680150113018.

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34

Chim, Harvey, Husain al-Qattan, Herbert Valencia, Carole Brathwaite, Andrew Price, and John A. I. Grossman. "Intravenous Glomus Tumor Masquerading as Lateral Antebrachial Cutaneous Neuroma." HAND 12, no. 2 (2016): NP19—NP21. http://dx.doi.org/10.1177/1558944716675296.

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Background: Intravenous glomus tumors are extremely rare. Methods: We report a patient with an intravenous glomus tumor within a venous aneurysm misdiagnosed as a neuroma of the lateral antebrachial cutaneous nerve, based on clinical exam, electrodiagnostic studies, and findings on a magnetic resonance imaging neurogram. Results: After surgical resection, the patient’s symptoms, including pain and localized hypersensitivity, totally resolved. Conclusions: This case illustrates 2 important points. First, unlike extradigital glomus tumors, magnetic resonance imaging is not reliable in diagnosing

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35

Bourgeault, Emilie, Jimmy Alain, and Eric Gagné. "Primary Cutaneous Carcinosarcoma of the Basal Cell Subtype Should Be Treated as a High-Risk Basal Cell Carcinoma." Journal of Cutaneous Medicine and Surgery 19, no. 4 (2015): 407–11. http://dx.doi.org/10.1177/1203475415575233.

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Background: Cutaneous carcinosarcoma is a rare primary tumor of the skin, characterized by biphasic epithelial and mesenchymal differentiation. Objective: Due to the limited number of cases reported, there is no consensus regarding treatment and prognosis. Some authors suggest that cutaneous carcinosarcomas should be viewed as aggressive tumors, with ancillary imaging used to evaluate potential metastatic disease. Other reports demonstrate an indolent disease course, especially with epidermal-type cutaneous carcinosarcomas. Methods: We report a case of cutaneous carcinosarcoma, which we treate

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Gorbachev, Anton, Marianne Petro, and Robert Fairchild. "Immune stress-induced generation of tumor variants deficient in CXCL9/Mig expression (100.11)." Journal of Immunology 184, no. 1_Supplement (2010): 100.11. http://dx.doi.org/10.4049/jimmunol.184.supp.100.11.

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Abstract Mechanisms promoting expansion of non-melanoma skin cancers remain poorly understood. Studies using a murine model of cutaneous fibrosarcoma demonstrated that although primary tumor growth is suppressed by IFN-g-dependent host immunity, the tumor eventually escapes this immunosurveillance. To investigate mechanisms of this process we used ELISPOT assays to demonstrate that the ability of tumor cells to produce the IFN-g-inducible chemokine CXCL9/Mig decreased during progression of cutaneous fibrosarcomas in immunocompetent wild type mice, but not in immunodeficient RAG1-/- mice. Tumor

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SATBAYEVA, E. B., N. A. MUCHAMETGALIEV, and E. E. ISKAKOVA. "Cutaneous leiomyosarcoma/ atypical smooth muscle sarcoma." Oncologia i radiologia Kazakhstana 56, no. 2 (2020): 16–18. http://dx.doi.org/10.52532/2663-4864-2020-2-56-16-18.

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Relevance: Cutaneous leiomyosarcoma is a rare primary dermal neoplasm, accounting for up to 2-3% of all superficial sarcomas. It can occur at any age, most likely between the ages of 50 and 70 years. This tumor has a high recurrence potential in case of insufficiently deep excision. Recurrent tumors are more aggressive and characterized by subsequent metastasis. The purpose of the study was to demonstrate the results of the histopathological examination of a cutaneous leiomyosarcoma / atypical smooth muscle tumor. Results: Cutaneous leiomyosarcoma was represented

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Izawa, T., J. Yamate, S. Takeda, D. Kumagai, and M. Kuwamura. "Cutaneous Rhabdoid Tumor in a Cat." Veterinary Pathology 45, no. 6 (2008): 897–900. http://dx.doi.org/10.1354/vp.45-6-897.

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Rhabdoid tumor is a highly aggressive neoplasm of unknown cellular origin in humans, usually occurring in the kidney and central nervous system of infants or children. In older patients, it occurs rarely in other organs, including the skin and soft tissues. A subcutaneous mass in a 13-year-old male mixed-breed cat was composed of nests or sheets of round to polygonal cells with glassy eosinophilic cytoplasmic inclusions. Immunohistochemically, many neoplastic cells expressed vimentin, localized to the cytoplasmic inclusions, whereas the cytoplasm of some neoplastic cells was diffusely positive

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Bavikar, Rupali, Yamini Ingale, Prachi Chouhan, and Iqbal Banyameen. "Keratoacanthoma: An Underreported Tumor." Medical Journal of Dr. D.Y. Patil Vidyapeeth 18, no. 2 (2025): 356–58. https://doi.org/10.4103/mjdrdypu.mjdrdypu_151_24.

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ABSTRACT Keratoacanthoma (KA) is a common but underreported tumor of the skin. It is a common cutaneous neoplasm. The most common sites are sun-exposed skin in light-skinned persons of middle age or older. It is considered the prototype of cutaneous pseudo-malignancies. Histopathological verification is done for the diagnosis. The role of radiation therapy and chemical application have not been proven yet. Complete surgical excision is the gold standard for all types of KA.

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Kai, Hiromichi, Takafumi Kadono, Hanako Ohmatsu, et al. "Beta7 integrin deficiency suppress cutaneous tumor formation (101.15)." Journal of Immunology 184, no. 1_Supplement (2010): 101.15. http://dx.doi.org/10.4049/jimmunol.184.supp.101.15.

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Abstract Beta7 integrin, a cell adhesion molecule, associates either with the alpha4 or with the alphaE integrin subunit. Alpha4beta7 integrin is expressed on most leucocytes and is essential for their migration to gut-associated lymphoid tissues by interacting with its primary ligand, MAdCAM-1. Although involvement of beta7 integrin in intestinal immunity is well-established, little has been known about the engagements of beta7 integrin in cutaneous immune responses, especially cutaneous anti-tumor immunity. In this study, we injected B16 murine melanoma cells into the skin superficial to the

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Ndiaye Diop, MT, B. Seck, K. Diop, et al. "Rapidly fatal anaplastic CD30+ primary cutaneous T-cell lymphoma: about a case." Journal Africain des Cas Cliniques et Revues 9, no. 1 (2025): 176–80. https://doi.org/10.70065/2591.jaccrafri.003l011503.

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CD30+ anaplastic primary cutaneous T-cell lymphoma is a type of cutaneous lymphoma rarely described in the literature and has an exceptional disseminated tumor form. This was a 73-year-old man who presented with nodular skin tumors whose size exceeded 5 cm, firm, painless, secondarily ulcerated, becoming ulcerative budding with a necrotic-purulent background and very painful. These lesions were located on the lower limbs, predominant on the right. Extra-dermatological examination found: right satellite tumor macropolyadenopathy, popliteal, inguinal, axillary and cervical. The rest of the physi

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McEvenue, Giancarlo, Ashley Kim, and Paul Binhammer. "Surgical Excision of Mycosis Fungoides Using Thumb-Sparing Reconstruction." HAND 12, no. 2 (2016): NP22—NP26. http://dx.doi.org/10.1177/1558944716669085.

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Background: The differential for soft tissue tumors of the hand and upper limb is broad. Hematologic malignancy remains quite low on the differential for soft tissue tumors involving the hand, and there is little in the literature describing surgical management of such cutaneous manifestations. When the tumor is large or involves the thumb, careful consideration of reconstructive options is required. Methods: We present a rare case of an aggressively enlarging mycosis fungoides, a cutaneous T-cell lymphoma tumor, involving the thumb. This tumor had a history of multiple failed treatment attemp

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Titov, K. S., A. A. Markin, E. I. Schurygina, N. S. Karnaukhov, D. A. Zaryanov, and D. N. Bubenko. "Morphological and immunohistochemical analysis of tumor-infiltrating lymphocytes, M2 macrophages, BCL 6 and SOX10 in the tumor microenvironment of nodular cutaneous melanoma." Head and Neck Tumors (HNT) 13, no. 1 (2023): 65–74. http://dx.doi.org/10.17650/2222-1468-2023-13-1-65-74.

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Introduction. Cutaneous melanoma is one of the most aggressive malignant tumors, and its nodular form with vertical growth is characterized by unfavorable prognosis. However, in the recent years due to advances in basic oncology, a breakthrough in drug therapy of this pathology was made. To a great extent, it is linked to implementation of new therapy with checkpoint inhibitors. The best and longest response rates of cutaneous melanoma to this treatment were achieved compared to other oncological diseases. This fact can be explained by immunogenicity of cutaneous melanoma, high mutational load

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Satbayeva, E. B., N. A. Muchametgaliev, and E. E. Iskakova. "Cutaneous leiomyosarcoma / atypical smooth muscle sarcoma." Oncologia i radiologia Kazakhstana 56, no. 2 (2020): 22–25. http://dx.doi.org/10.52532/2521-6414-2020-2-56-22-25.

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Relevance: Cutaneous leiomyosarcoma is a rare primary dermal neoplasm, accounting for up to 2-3% of all superficial sarcomas. It can occur at any age, most likely between the ages of 50 and 70 years. This tumor has a high recurrence potential in case of insufficiently deep excision. Recurrent tumors are more aggressive and characterized by subsequent metastasis. The purpose of the study was to demonstrate the results of the histopathological examination of a cutaneous leiomyosarcoma / atypical smooth muscle tumor. Results: Cutaneous leiomyosarcom

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Hauch, Adam T., Joseph F. Buell, Margit McGowan, et al. "Cutaneous Metastases from Primary Hepatobiliary Tumors as the First Sign of Tumor Recurrence following Liver Transplantation." Case Reports in Transplantation 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/838949.

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Cutaneous metastasis from hepatobiliary tumors is a rare event, especially following liver transplantation. We report our experience with two cases of cutaneous metastases from both hepatocellular carcinoma and mixed hepatocellular/cholangiocarcinoma following liver transplantation, along with a review of the literature.

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Kashani-Sabet, Mohammed, Richard W. Sagebiel, Carlos M. M. Ferreira, Mehdi Nosrati, and James R. Miller. "Tumor Vascularity in the Prognostic Assessment of Primary Cutaneous Melanoma." Journal of Clinical Oncology 20, no. 7 (2002): 1826–31. http://dx.doi.org/10.1200/jco.2002.07.082.

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PURPOSE: The vascular supply of the primary tumor is recognized to play an important role in the progression of a number of solid tumors. However, the role of tumor vascularity in the prognostic assessment of melanoma remains unclear. The purpose of this study was to determine the prognostic impact of patterns of vascularity on the outcome associated with cutaneous melanoma. PATIENTS AND METHODS: Tumor vascularity was documented prospectively using routine histopathologic analysis of 417 primary cutaneous melanomas from the University of California at San Francisco Melanoma Center database. Fo

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de Nardi, Andrigo Barboza, Rodrigo dos Santos Horta, Carlos Eduardo Fonseca-Alves, et al. "Diagnosis, Prognosis and Treatment of Canine Cutaneous and Subcutaneous Mast Cell Tumors." Cells 11, no. 4 (2022): 618. http://dx.doi.org/10.3390/cells11040618.

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Mast cell tumors (MCTs) are hematopoietic neoplasms composed of mast cells. It is highly common in dogs and is extremely important in the veterinary oncology field. It represents the third most common tumor subtype, and is the most common malignant skin tumor in dogs, corresponding to 11% of skin cancer cases. The objective of this critical review was to present the report of the 2nd Consensus meeting on the Diagnosis, Prognosis, and Treatment of Canine Cutaneous and Subcutaneous Mast Cell Tumors, which was organized by the Brazilian Association of Veterinary Oncology (ABROVET) in August 2021.

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Diaz, Michael J., Angela Fadil, Jasmine T. Tran, et al. "Primary and Metastatic Cutaneous Melanomas Discriminately Enrich Several Ligand-Receptor Interactions." Life 13, no. 1 (2023): 180. http://dx.doi.org/10.3390/life13010180.

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Introduction: Cutaneous melanoma remains a leading cancer with sobering post-metastasis mortality rates. To date, the ligand-receptor interactome of melanomas remains weakly studied despite applicability to anti-cancer drug discovery. Here we leverage established crosstalk methodologies to characterize important ligand-receptor pairs in primary and metastatic cutaneous melanoma. Methods: Bulk transcriptomic data, representing 470 cutaneous melanoma samples, was retrieved from the Broad Genome Data Analysis Center Firehose portal. Tumor and stroma compartments were computationally derived as a

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Duncan, Lyn M., James Deeds, Frank E. Cronin, et al. "Melastatin Expression and Prognosis in Cutaneous Malignant Melanoma." Journal of Clinical Oncology 19, no. 2 (2001): 568–76. http://dx.doi.org/10.1200/jco.2001.19.2.568.

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PURPOSE: Melastatin (MLSN-1), a novel melanocyte-specific gene recently identified using a genomic approach, is expressed in murine and human melanoma cells at levels inversely proportional to metastatic rates in vivo. We studied the relationship between expression of melastatin mRNA in the primary cutaneous tumor and prognosis in patients with localized malignant melanoma. PATIENTS AND METHODS: Melastatin mRNA was evaluated by in situ hybridization in primary cutaneous melanoma from 150 patients with localized disease (American Joint Committee on Cancer [AJCC] stage I and II). Multivariate Co

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Hail, Kamel, Radia Benyahia, Lounas Benghanem, Nabil Bellik, and Nazim Laraba. "Clinical Management of Male Breast Cancer with A Single Metachronous Cutaneous Metastasis: A Case Report and Review." SAR Journal of Medical Case Reports 4, no. 05 (2023): 63–66. http://dx.doi.org/10.36346/sarjmcr.2023.v04i05.002.

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Any cancer can spread to the skin, a phenomenon typically more common in advanced stages of the disease. However, some tumors can remain clinically silent until the discovery of a cutaneous metastasis, often complicating the diagnosis of the primary tumor, especially if it's a rare tumor like breast cancer in men. It is in this context that we report a case of localized cutaneous metastasis on the scalp, without the presence of other associated clinical signs. Investigations revealed a metastatic breast carcinoma requiring extensive surgical intervention, complemented by adjuvant treatments.

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