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Journal articles on the topic 'Apocrifo'

Author: Grafiati

Published: 11 March 2023

Last updated: 31 July 2025

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1

Ramelli, Ilaria. "L'epistolario Seneca-san Paolo: veramente apocrifo?" Theologica Leoniana 2, no. 2 (2013): 115–53. https://doi.org/10.5281/zenodo.13765321.

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Il mito di Seneca cristiano nacque soltanto nel primissimo umanesimo, come aveva già supposto Momigliano e come hanno confermato e precisato Guido Billanovich e Agostino Sottili, sottoponendo all’attenzione degli studiosi le considerazioni sul cristianesimo di Seneca svolte da Rolando da Piazzola e da Albertino Mussato, del circolo preumanistico padovano. Mussato scrisse una biografia di Seneca, in cui è asserito il cristianesimo del filosofo, in base a Hier. Vir. Ill. 12, e a due passi dell’epistolario con Paolo, Epp. I e VII, da cui emerge la convinzione di Seneca c

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2

den Boeft, J., and Laura Bocciolini Palagi. "Epistolario apocrifo di Seneca e San Paolo." Vigiliae Christianae 42, no. 2 (1988): 194. http://dx.doi.org/10.2307/1583921.

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3

Attisani, Antonio. "Acta Gnosis." TDR/The Drama Review 52, no. 2 (2008): 75–106. http://dx.doi.org/10.1162/dram.2008.52.2.75.

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In this selection from Un teatro apocrifo, Attisani goes beyond previous academic acknowledgments of Grotowski's interest in Gnostic texts, tracing the influence of key materials found in the Nag Hammadi and the significance of Gnostic belief as a secret subcurrent in the 20th-century theatrical avantgarde.

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4

Carusi, Paola. "Sirr al-ʿālamayn: un Ġazālī apocrifo o inaspettato?" Studi Magrebini 17, № 1-2 (2019): 32–74. http://dx.doi.org/10.1163/2590034x-12340004.

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Abstract Sirr al-ʿālamayn wa kašf mā fī’l-dārayn is a work whose attribution to al-Ġazālī has long been debated, and whose authenticity today is almost unanimously denied. In what may be considered as its second part, it contains some passages relating to alchemy and its operations that seem to be worthy of reflection. Such passages, present in a work attributed to Ġazālī, do not necessarily cast further doubts on its attribution; because if on the one hand some passages are to be considered perhaps a bit too ‘audacious’, on the other a non-negligible part of the work is dedicated to Ġazalian

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5

Surace, Bruno. "OcchioPinocchio. Il Pinocchio apocrifo – e maledetto – di Francesco Nuti." Schermi. Storie e culture del cinema e dei media in Italia 7, no. 13 (2023): 63–79. http://dx.doi.org/10.54103/2532-2486/21277.

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Severely criticized almost unanimously at the time of its release, Francesco Nuti’s “OcchioPinocchio” (1994) represents a rare case of a “cursed” Italian film from the 1990s. It became notorious for its extremely costly and troubled production, whose release was delayed by a year, as well as for the massive flop that followed, so severe that it marked the decline of Nuti’s career and personal life, despite his previous success as a comedian and director. Twenty years after its release, perhaps it is time to reevaluate its worth, if not critically, then at least by scientifically identifying th

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6

Zarzeczny, Rafał. "Pneumatologia Hierakasa z Egiptu na tle apokryficznego "Wniebowstąpienia Izajasza" i starożytnych tradycji melchizedekiańskich." Vox Patrum 49 (June 15, 2006): 735–48. http://dx.doi.org/10.31743/vp.8248.

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Insegnamento di Ieraca di Leontopolis in Egitto sullo Spirito Santo, secondo un testimonio d’Epifanio, vescovo di Salamina, si richiama ad un testo apocrifo giudeo-cristiano, detto Ascensione d’Isaia, dove la Seconda Persona fu descritta come un angelo. Un alto tratto della stessa dottrina mette in rapporto lo Spirito Santo con Melchisedek, in modo che il re biblico divenne un’ipostasi dello Spirito divino. Simili ritratti si possono trovare nella letteratura cristiana anticha (Ambrosiastro, Girolamo, Cirillo d’Alessandria) ed anche quella giudaica dal periodo postbiblico (Qumran).

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7

Rossi, Federico. "Le Meditationes vitae Christi in volgare in due codici miscellanei (Ricc. 1346, Ricc. 1341)." Specula Revista de Humanidades y Espiritualidad 12, no. 1 (2025): 67–89. https://doi.org/10.46583/specula_2025.12.1128.

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L’articolo prende in esame due codici che trasmettono redazioni volgari delle Meditationes vitae Christi nel contesto di raccolte devozionali più complesse. Il Riccardiano 1346 presenta una selezione di capitoli delle Meditationes che riguardano quasi soltanto la vita pubblica di Cristo; questa peculiare selezione trova spiegazione in una nota del compilatore. Il codice trasmette inoltre il Colloquio spirituale di Simone da Cascina e un volgarizzamento dell’omelia pseudo-origeniana sulla Maddalena, distinto da tutte le altre versioni note. Il Riccardiano 1341 inserisce invece le Meditationes n

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8

García, Lorena Gómez, and Alberto Sabando Carranza. "Hidrocistoma apocrino." FMC - Formación Médica Continuada en Atención Primaria 18, no. 4 (2011): 238–39. http://dx.doi.org/10.1016/s1134-2072(11)70094-9.

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9

Teresa Ganún, María, Raúl Villa, and Daniel Ciocca. "Cistoadenoma apocrino." Piel 19, no. 4 (2004): 206–9. http://dx.doi.org/10.1016/s0213-9251(04)72832-4.

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10

Ruiz-Villaverde, Ricardo, Manuel Galán-Gutierrez, Husein Husein-Elahmed, and Jose María Martinez de Victoria. "Hidroadenocarcinoma apocrino." Piel 28, no. 10 (2013): 620–22. http://dx.doi.org/10.1016/j.piel.2013.04.009.

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11

Holdridge, Jefferson, Elena Sanz Ortega, and Cristina Toledo Baez. "Apocrypha / Apocrifos." Sirena: poesia, arte y critica 2006, no. 1 (2006): 110–11. http://dx.doi.org/10.1353/sir.2006.0052.

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12

SATO, Noriko, Akiko FUKUSHIMA, Yumiko KUBOTA, and Juichiro NAKAYAMA. "Apocrine Hidrocystoma." Nishi Nihon Hifuka 70, no. 4 (2008): 369–70. http://dx.doi.org/10.2336/nishinihonhifu.70.369.

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13

Ginarte Val, Manuel, Benigno Monteagudo Sánchez, Carmen Peteiro García, and Jaime Toribio Pérez. "Adenoma tubular apocrino." Actas Dermo-Sifiliográficas 94, no. 1-2 (2003): 99–101. http://dx.doi.org/10.1016/s0001-7310(03)79233-3.

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14

Monteagudo, Benigno, Iosu M. Antón-Badiola, María J. Muñoz, Carmen Paredes-Suárez, and Manuel Vázquez-Blanco. "Hidroadenoma apocrino pigmentado." Actas Dermo-Sifiliográficas 96, no. 1 (2005): 50–51. http://dx.doi.org/10.1016/s0001-7310(05)73034-9.

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15

Asirvatham, Jaya Ruth, Maria Monica Garcia Falcone, and Celina G. Kleer. "Atypical Apocrine Adenosis: Diagnostic Challenges and Pitfalls." Archives of Pathology & Laboratory Medicine 140, no. 10 (2016): 1045–51. http://dx.doi.org/10.5858/arpa.2016-0238-ra.

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Apocrine change in the breast is an extremely common finding. In most cases, the benign or malignant nature of the lesion is easily recognized. Apocrine adenosis is used to describe sclerosing adenosis with apocrine change. The term apocrine atypia is used when there is significant cytologic atypia in apocrine cells, characterized by a 3-fold nuclear enlargement, prominent/multiple nucleoli, and hyperchromasia. Atypical apocrine adenosis is diagnosed when apocrine adenosis and apocrine atypia are superimposed. However, there are no definite criteria to distinguish atypical apocrine adenosis fr

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Trenkic, Srbobran, Vuka Katic, Mitsa Pashalina, Vesna Zivkovic, Maja Milentijevic, and Milos Kostov. "The histologic spectrum of apocrine lesions of the breast." Archive of Oncology 12, no. 1 (2004): 61–65. http://dx.doi.org/10.2298/aoo0401061t.

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New data on apocrine carcinoma of the breast, especially on its unusual pathogenesis, are the facts that justify this study. The aim of this study was to describe the morphological features in both benign apocrine lesions and invasive apocrine carcinomas of the breast. The following apocrine lesions were pointed out: cysts, metaplasia, adenosis, adenoma, borderline malignant lesion, intraductal carcinoma and invasive apocrine carcinoma. Surgical specimens of breast benign and malignant lesions were fixed in formalin, embedded in paraffin blocks and the slides were stained with HE, PAS and immu

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17

Visscher, Daniel W. "Apocrine Ductal Carcinoma In Situ Involving a Sclerosing Lesion With Adenosis: Report of a Case." Archives of Pathology & Laboratory Medicine 133, no. 11 (2009): 1817–21. http://dx.doi.org/10.5858/133.11.1817.

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Abstract Apocrine metaplasia is a ubiquitous component of the mammary fibrocystic change spectrum. Although mostly associated with cysts, apocrine metaplasia can also present as a proliferative lesion, rarely with cytologic atypism. Apocrine atypia is characterized by 3-fold nuclear enlargement, multiple nucleoli, and hyperchromatism and generally arises in florid adenosis or radial sclerosing lesions. Dramatic apocrine atypia may be very difficult to distinguish from apocrine ductal carcinoma in situ. The latter is distinguished from apocrine atypia by greater extent of the lesion (&gt;0.

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18

YATES, A. J., and A. AHMED. "Apocrine carcinoma and apocrine metaplasia." Histopathology 13, no. 2 (1988): 228–31. http://dx.doi.org/10.1111/j.1365-2559.1988.tb02030.x.

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19

D'Arcy, Clare, and Cecily Quinn. "Apocrine lesions of the breast: part 1 of a two-part review: benign, atypical and in situ apocrine proliferations of the breast." Journal of Clinical Pathology 72, no. 1 (2018): 1–6. http://dx.doi.org/10.1136/jclinpath-2018-205484.

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Apocrine morphology is a common phenomenon encountered in everyday breast pathology practice, and is defined as cuboidal or columnar cells exhibiting abundant eosinophilic granular cytoplasm, prominent apical granules, a low nuclear-cytoplasmic ratio, and round nuclei with pale chromatin and prominent nucleoli. Apocrine morphology is recognised in benign, atypical and malignant lesions of the breast. The morphology of apocrine atypia and non-high-grade apocrine ductal carcinoma in situ (DCIS) is less well defined due to the relative rarity of these lesions. In part 1 of this two-part review, w

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20

Segura-Sánchez, Juan, Carmen Eloy García-Carrasco, and Carlos Escudero-Severín. "Dermatofibroadenoma apocrino hemosiderótico/quiste glandular apocrino con estroma similar al dermatofibroma hemosiderótico." Revista Española de Patología 50, no. 4 (2017): 253–56. http://dx.doi.org/10.1016/j.patol.2016.05.001.

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21

Kito, Katsumi, Toshiharu Maeda, Keiko Ninomiya, et al. "HER2-Positive Metaplastic Spindle Cell Carcinoma Associated with Synchronous Bilateral Apocrine Carcinoma of the Breast." Case Reports in Pathology 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/310829.

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Apocrine carcinoma, which is strictly defined as over 90% of tumor cells showing apocrine differentiation, is a rare variant of breast cancer. Here we report an uncommon case in which apocrine carcinomas developed concurrently in both breasts; in addition, a sarcomatoid spindle cell lesion was coincident in the right breast. Both apocrine carcinomas were immunohistochemically negative for estrogen receptor (ER) and progesterone receptor (PgR), but diffusely positive for androgen receptor (AR), GCDFP-15, and HER2. The presence of intraductal components in bilateral carcinomas and the absence of

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22

Fuehrer, Neil, Lynn Hartmann, Amy Degnim, et al. "Atypical Apocrine Adenosis of the Breast: Long-term Follow-up in 37 Patients." Archives of Pathology & Laboratory Medicine 136, no. 2 (2012): 179–82. http://dx.doi.org/10.5858/arpa.2011-0225-oa.

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Context.—Atypical apocrine adenosis is a rare breast lesion in which the cellular population demonstrates cytologic alterations that may be confused with malignancy. The clinical significance and management of atypical apocrine adenosis are unclear because of the lack of long-term follow-up studies. Objective.—To determine the breast cancer risk in a retrospective series of patients with atypical apocrine adenosis diagnosed in otherwise benign, breast excisional biopsies. Design.—We identified 37 atypical apocrine adenosis cases in the Mayo Benign Breast Disease Cohort (9340 women) between 196

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23

Benigni, Giuliana, and Francesco Squartini. "Uneven Distribution and Significant Concentration of Apocrine Metaplasia in Lower Breast Quadrants." Tumori Journal 72, no. 2 (1986): 179–82. http://dx.doi.org/10.1177/030089168607200210.

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Two hundred human breasts removed for clinical cancer by radical mastectomy were analyzed to determine whether apocrine metaplasia and apocrine cysts have predilective sites in the four mammary quadrants. One block of tissue randomly removed for each quadrant was examined in one or more histologic sections. The results showed a concentration of apocrine metaplasia and apocrine cysts in the lower mammary quadrants (17.5% versus 8.2%), which is highly significant (x2 = 15.25; P < 0.001). The different distribution between breast cancer (showing predilection for the upper quadrants) and apocri

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24

Trillos Campuzano, Karen Alejandra. "Hidrocistoma apocrino palpebral y diagnósticos diferenciales más representativos." Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica 33, no. 1 (2025): 53–58. https://doi.org/10.29176/2590843x.1891.

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El hidrocistoma apocrino es un tumor quístico benigno que se deriva de las glándulas sudoríparas apocrinas. Su localización más frecuente ocurre a nivel palpebral en donde también es conocido como quiste de Moll. Usualmente se describe como una lesión nodular translúcida en forma de cúpula, con una coloración y un tamaño variables lo que puede dificultar el diagnóstico diferencial. Se hace una revisión sobre las características clínicas más importantes del hidrocistoma apocrino y su diferenciación con otras lesiones similares a nivel palpebral.

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25

Wader, Jyotsna V., Akash Jain, Suresh J. Bhosale, Pandurang G. Chougale, and Sujata S. Kumbhar. "Apocrine Carcinoma of Breast: A Case Report with Review of the Literature." Case Reports in Pathology 2013 (2013): 1–3. http://dx.doi.org/10.1155/2013/170918.

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Apocrine carcinoma is a very rare form of breast malignancy with an incidence of <1% of female invasive breast carcinoma. We report a case of apocrine carcinoma in a 42-year female with marked adenosis showing apocrine metaplasia and discuss the criteria to diagnose apocrine carcinoma with the emerging concept of androgen receptor positivity with its implication on treatment and management of the patient.

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26

DE FONTAINE, S., J. VAN GEERTRUYDEN, and E. VANDEWEYER. "Apocrine Hidrocystoma of the Finger." Journal of Hand Surgery 23, no. 2 (1998): 281–82. http://dx.doi.org/10.1016/s0266-7681(98)80199-x.

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An apocrine hidrocystoma occurring on the finger of a 55-year-old man is reported. The lesion presented as a solitary, painless cystic nodule on the dorsal aspect of the middle phalanx of the index finger. Apocrine hidrocystoma is a benign tumour developed from apocrine sweat glands, but the location of the lesion was, however, not consistent with reported locations of apocrine glands in the adult.

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D'Arcy, Clare, and Cecily M. Quinn. "Apocrine lesions of the breast: part 2 of a two-part review. Invasive apocrine carcinoma, the molecular apocrine signature and utility of immunohistochemistry in the diagnosis of apocrine lesions of the breast." Journal of Clinical Pathology 72, no. 1 (2018): 7–11. http://dx.doi.org/10.1136/jclinpath-2018-205485.

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Pure apocrine carcinoma of the breast is rare and has been defined by using a combination of morphologic (apocrine morphology in >90% of tumour cells) and immunohistochemical criteria (oestrogen receptor (ER) and progesterone receptor (PR) negative and androgen receptor (AR) positive). Recent advances in the molecular classification of breast tumours have uncovered a subset of breast tumours associated with high expression of androgen receptor mRNA including the so-called ‘luminal androgen receptor (LAR) tumours’ and ‘molecular apocrine tumours’ (MATs). Recognition of these tumour subsets h

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28

Wu, Shang-Yen, Jin-Wei Huang, Yuan-Chieh Lee, Fang-Ling Chang, Ming-Hsun Li, and Nancy Chen. "Apocrine Hidrocystoma with IgG4 Plasma Cell Infiltration Presenting as Recurrent Chalazion: A Case Report." Medicina 58, no. 7 (2022): 840. http://dx.doi.org/10.3390/medicina58070840.

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Apocrine hidrocystomas are benign cystic tumors resulting from apocrine sweat glands’ proliferation. They typically present as solitary, slow-growing nodules at the head and neck, especially in the periorbital cutaneous region. We present a case of periorbital apocrine hidrocystoma in a 22-year-old woman that was treated as chalazion previously. Besides the hallmark histopathological findings of apocrine hidrocystoma, IgG4 plasma cell infiltration of the cystic wall was also found. The ratio of IgG4-to-IgG-positive plasma cells was high, whereas serum IgG4 was within the standard limit. This i

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C. A., Shashirekha, Krishnaprasad ., Sandeep Reddy, et al. "Diagnostic dilemma in skin adnexa malignancy: a rare case report with review of literature." International Surgery Journal 5, no. 5 (2018): 1956. http://dx.doi.org/10.18203/2349-2902.isj20181618.

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Apocrine malignancies are rare to occur. Axilla and the anogenital skin are the most common sites of primary tumour. Apocrine malignancy carries high risk of lymphatic and vascular spreading to lung, liver and bone. A 40 years old painter, presents with diffuse swelling and pain in the left lower limb up to left inguinal region since 5 to 6 months. With generalised lymphadenopathy. On evaluation, revealed adenocarcinoma of apocrine, skin adnexa in the extremities of the limb with extensive distant metastasis. Apart from Dermatologists other board specialty consultant should be aware of the pos

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30

Oeyen, Jan Philip, Patrice Baa-Puyoulet, Joshua B. Benoit, et al. "Sawfly Genomes Reveal Evolutionary Acquisitions That Fostered the Mega-Radiation of Parasitoid and Eusocial Hymenoptera." Genome Biology and Evolution 12, no. 7 (2020): 1099–188. http://dx.doi.org/10.1093/gbe/evaa106.

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Abstract The tremendous diversity of Hymenoptera is commonly attributed to the evolution of parasitoidism in the last common ancestor of parasitoid sawflies (Orussidae) and wasp-waisted Hymenoptera (Apocrita). However, Apocrita and Orussidae differ dramatically in their species richness, indicating that the diversification of Apocrita was promoted by additional traits. These traits have remained elusive due to a paucity of sawfly genome sequences, in particular those of parasitoid sawflies. Here, we present comparative analyses of draft genomes of the primarily phytophagous sawfly Athalia rosa

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Pinheiro, Jorge Adriano Ferreira, and José Manuel Pedrosa Baptista Lopes. "Periocular Sebaceous Carcinoma With Apocrine Differentiation: A Case Report and Review of the Literature." International Journal of Surgical Pathology 27, no. 4 (2018): 432–36. http://dx.doi.org/10.1177/1066896918816806.

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A 61-year-old man presented with a dome-shaped tumor in the right eyelid. Histology revealed a cutaneous neoplasm with lobular growth pattern. It was composed of large basaloid cells, cells with sebaceous differentiation, and glandular structures with apocrine features. The immunohistochemical study revealed diffuse expression of CK7, EMA, and androgen receptors in the neoplastic cells. Gross cystic disease fluid protein-15 highlighted the luminal cells, consistent with apocrine differentiation. These findings fit with a sebaceous carcinoma with focal glandular apocrine differentiation (“sebo-

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García Hernández, Felip, Enric Piqué Durán, and Miquel Casals Andreu. "Hidrocistoma apocrino sobre nevus sebáceo." Actas Dermo-Sifiliográficas 94, no. 1-2 (2003): 113–15. http://dx.doi.org/10.1016/s0001-7310(03)79237-0.

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Torres Fuentes, Carlos Eduardo, Claudia Bolaños Arturo, Giovanni Montealegre, and Marian Rolón. "Acrospiroma apocrino en la mano." Piel 27, no. 5 (2012): 292–94. http://dx.doi.org/10.1016/j.piel.2010.12.020.

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34

Lusini, Gianfrancesco. "Gli Atti apocrifi di Marco." Aethiopica 12 (April 7, 2012): 7–47. http://dx.doi.org/10.15460/aethiopica.12.1.92.

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The apocryphal Acts of Mark (Gädlä Marqos) were translated from Greek in Ethiopic in the last years of the reign of ʿEzana, between 360 and 370. They are transmitted only by two manuscripts: EMML 1763, ff. 224–227 (=A), dated 1336/37 or 1339/40 and pub-lished by Getatchew Haile, “A new Ethiopic version of the Acts of St. Mark (EMML 1763, ff. 224r–227r)”, Analecta Bollandiana, 99, 1981, pp. 117–134; and Pistoia, Biblioteca Forteguerriana, ms. Martini etiop. n. 5 (= Zanutto n. 2), ff. 82–89 (= B), 18th–19th cent., recently discovered (G.L., “I codici etiopici del Fondo Martini nella Biblioteca F

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Karahan, S., D. Yildiz, and D. Bolat. "Scanning electron microscopic features of the ovine interdigital sinus." Acta Veterinaria Hungarica 55, no. 4 (2007): 417–24. http://dx.doi.org/10.1556/avet.55.2007.4.1.

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This article describes the scanning electron microscopic (SEM) features of the ovine interdigital sinus. The lumen was filled with a dense secretory material and quite a number of hairs embedded in the luminal content. For SEM purposes, the sinus was divided into three parts: base, body and neck. At the cut surface, the wall exhibited significant folds which were almost absent in the base, the very short blind end of the sinus. The wall had three layers: epidermis, dermis and fibrous capsule. Stratified epithelium with a prominent keratin layer faced the lumen. The inner surface was similar to

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Poli, Pier Paolo, Luca Creminelli, Valeria Moramarco, Alessandro Del Gobbo, Franco Ferrante, and Carlo Maiorana. "Diagnostic Workup and Treatment of a Rare Apocrine Hidrocystoma Affecting the Oral Mucosa: A Clinical and Histological Case Report." Case Reports in Dentistry 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/9382812.

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Apocrine hidrocystomas are rare benign cystic tumors originating from the secretory portion of apocrine sweat glands. To the best of our knowledge, there is no evidence currently available reporting the presence of apocrine hidrocystomas in the oral cavity. Therefore, this case report aims to describe the clinical and histological features of an apocrine hidrocystoma affecting the oral mucosa. A 69-year-old male patient presented with a 1-year history of a solitary, well-circumscribed, submucosal mass in the left posterior buccal mucosa. The clinical examination revealed a yellowish soft, fluc

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37

Bommakanti, Janardhan, and Mahjabeen Salma. "Apocrine hidrocystoma." Indian Journal of Dermatopathology and Diagnostic Dermatology 2, no. 1 (2015): 26. http://dx.doi.org/10.4103/2349-6029.160988.

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38

Fukuda, Michio, Haruhisa Kato, and Toshio Hamada. "Apocrine Hidrocystoma." Journal of Dermatology 16, no. 4 (1989): 315–20. http://dx.doi.org/10.1111/j.1346-8138.1989.tb01271.x.

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Salas-Alanís, Jullio C., Mauricio Salas-Garza, María G. Moreno-Treviño, Raymundo Garza-Martínez, José G. Silva-Hernández, and Gerardo Rivera-Silva. "Apocrine miliaria." Medicina Clínica Práctica 7, no. 4 (2024): 100456. http://dx.doi.org/10.1016/j.mcpsp.2024.100456.

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40

Polat, M., M. Dikilitaş, A. Gözübüyükoğullari, and N. Alli. "Apocrine chromhidrosis." Clinical and Experimental Dermatology 34, no. 7 (2009): e373-e374. http://dx.doi.org/10.1111/j.1365-2230.2009.03327.x.

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Kim, Joong Hwan, Hoon Hur, Chang Woo Lee, and Young Tae Kim. "Apocrine nevus." Journal of the American Academy of Dermatology 18, no. 3 (1988): 579–81. http://dx.doi.org/10.1016/s0190-9622(88)80291-3.

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42

MORI, OSAMU, HIROSHI HACHISUKA, and YOICHIRO SASAI. "APOCRINE NEVUS." International Journal of Dermatology 32, no. 6 (1993): 448–49. http://dx.doi.org/10.1111/j.1365-4362.1993.tb02821.x.

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Shah, Aadarsh, Zoi Tsianou, Ravi Suchak, and Jack Mann. "Apocrine Chromhidrosis." American Journal of Dermatopathology 42, no. 10 (2020): e147-e148. http://dx.doi.org/10.1097/dad.0000000000001712.

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Sakamoto, Fumiko, Masaaki Ito, Shinsuke Sato, and Yoshio Sato. "Basal cell tumor with apocrine differentiation: Apocrine epithelioma." Journal of the American Academy of Dermatology 13, no. 2 (1985): 355–63. http://dx.doi.org/10.1016/s0190-9622(85)70174-0.

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Abdel, Selim. "Understanding Apocrine Metaplasia of the Breast: A Closer Look at a Complex Phenomenon." Mega Journal of Case Reports 7, no. 3 (2024): 2001–3. https://doi.org/10.5281/zenodo.10894634.

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AbstractThis editorial provides a comprehensive exploration of apocrine metaplasia in the breast, delving into its clinicalimplications, diagnostic challenges, and potential causes. While generally benign, apocrine metaplasia posesdifficulties in accurate diagnosis due to its resemblance to more serious conditions. The editorial emphasizes theimportance of distinguishing apocrine metaplasia through advanced imaging and molecular studies and discussesongoing research into its hormonal and genetic underpinnings. With a focus on patient management andsurveillance, the editorial underscores the ne

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Pasquale-Styles, Melissa A., and Clara Milikowski. "Three-Millimeter Apocrine Adenoma in a Man: A Case Report and Review of the Literature." Archives of Pathology & Laboratory Medicine 127, no. 11 (2003): 1498–500. http://dx.doi.org/10.5858/2003-127-1498-taaiam.

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Abstract We describe a rare case of apocrine adenoma of the breast in a 45-year-old man. The patient presented with a tender lump in his left breast that had been present for 6 months. A mammogram identified a 3-mm nodular density in the breast, which was described as a hypoechoic nodule on ultrasound. Microscopic examination of tissue from an excisional biopsy revealed a 3-mm group of benign glands with abundant granular, eosinophilic cytoplasm and apical luminal blebbing, consistent with an apocrine adenoma. After reviewing other reported apocrine adenomas in the literature, we determined th

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Salama, Mohamed E., Muhammad Azam, Chan K. Ma, et al. "Chondroid Syringoma." Archives of Pathology & Laboratory Medicine 128, no. 9 (2004): 986–90. http://dx.doi.org/10.5858/2004-128-986-cs.

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Abstract Context.—Chondroid syringoma (CS) is a benign cutaneous adnexal tumor with epithelial and stromal components. Epithelial components derived from folliculo-sebaceous-apocrine germ are evident in apocrine but not in eccrine CS. Objectives.—To further characterize pilosebaceous differentiation and to identify the presence of Merkel cells in the areas of follicular differentiation. Design.—Histologic type, folliculo-sebaceous differentiation, character of stroma, and presence or absence of Merkel cells by cytokeratin (CK) 20 immunoreactivity were evaluated in 25 CSs (22 apocrine and 3 ecc

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Gianotti, Raffaele, Antonella Coggi, and Elvio Alessi. "Cutaneous Apocrine Mixed Tumor: Derived From the Apocrine Duct of the Folliculo-Sebaceous-Apocrine Unit?" American Journal of Dermatopathology 20, no. 3 (1998): 323–25. http://dx.doi.org/10.1097/00000372-199806000-00024.

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Moon, Chang-Hwan, Hyun-Ah Min, Hae-Beom Lee, Seong-Mok Jeong, and Dae-Hyun Kim. "Retroperitoneal Metastatic Apocrine Gland Ductal Adenocarcinoma in a Beagle Dog." Veterinary Sciences 9, no. 5 (2022): 234. http://dx.doi.org/10.3390/vetsci9050234.

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Tumors of sweat glands usually originate from apocrine glands and can develop throughout the body but are rare in dogs. This report describes the retroperitoneal metastasis of primary cutaneous apocrine adenocarcinoma. An 8-year-old, spayed female beagle dog, weighing 11.7 kg, presented with a history of anorexia, hypodynamia, and weight loss. Clinical examination, radiography, ultrasonography, and computed tomography revealed a skin mass on the dorsum of the right metatarsal region, an enlarged ipsilateral popliteal lymph node, and a retroperitoneal mass. Fine-needle aspiration cytology of th

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Hohšteter, Marko, Ivan-Conrado Šoštarić-Zuckermann, Ivana Mihoković Buhin, et al. "Expression of E-cadherin and Ki-67 in canine apocrine and sebaceous gland tumors." Veterinarski arhiv 91, no. 1 (2021): 51–63. http://dx.doi.org/10.24099/vet.arhiv.0778.

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A histopathological analysis of 13 apocrine gland tumors and 22 sebaceous gland tumors in dogs was performed, which were submitted to the Department of Veterinary Pathology from 1 January 2010 to 31 December 2012. An association between the immunohistochemical expression of E-cadherin and Ki-67, the type, and the biological behavior of the tumors was investigated. The mean age of dogs with apocrine gland tumors was 10.15 years, and 10.91 years for sebaceous gland tumors. According to the histopathological analysis, 53.8% carcinomas and 46.2% adenomas of the apocrine glands were found. In the s

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