Jump to content

Adrenocortical adenoma

From Wikipedia, the free encyclopedia
(Redirected from Adrenal adenoma, familial)
Adrenocortical Adenoma
Other namesAdrenal cortical adenoma, adrenal adenoma
Adrenal adenoma in a patient with Conn syndrome
SpecialtyEndocrinology, oncology Edit this on Wikidata

An adrenocortical adenoma or adrenal adenoma is commonly described as a benign neoplasm emerging from the cells that comprise the adrenal cortex. Like most adenomas, the adrenocortical adenoma is considered a benign tumor since the majority of them are non-functioning and asymptomatic. Adrenocortical adenomas are classified as ACTH-independent disorders, and are commonly associated with conditions linked to hyperadrenalism such as Cushing's syndrome (hypercortisolism) or Conn's syndrome (hyperaldosteronism), which is also known as primary aldosteronism.[1] In addition, recent case reports further support the affiliation of adrenocortical adenomas with hyperandrogenism or florid hyperandrogenism which can cause hyperandrogenic hirsutism in females.[2] "Cushing's syndrome" differs from the "Cushing's disease" even though both conditions are induced by hypercortisolism. The term "Cushing's disease" refers specifically to "secondary hypercortisolism" classified as "ACTH-dependent Cushing's syndrome" caused by pituitary adenomas. In contrast, "Cushing's syndrome" refers specifically to "primary hypercortisolism" classified as "ACTH-independent Cushing's syndrome" caused by adrenocortical adenomas.

Presentation

[edit]
Hypercortisolism
SpecialtyEndocrinology, oncology Edit this on Wikidata
SymptomsAdrenal Lesion

Adrenal adenomas are often categorized as endocrine-inactive tumors considering that majority of them are non-functioning and asymptomatic. Functional adrenocortical adenomas demonstrate symptoms consistent with mixed endocrine syndromes. In most reported cases of adrenocortical adenoma, patients have presented with one or multiple endocrine syndromes such as hyperaldosteronism/Conn's Syndrome,[3] hypercortisolism/Cushing's syndrome,[4] hyperandrogenism/feminization,[2] virilization,[5] or hirsutism.[6] Some of the common symptoms associated with adrenocortical adenomas include:

Musculoskeletal

Cardiovascular

Endocrine and Metabolic

→More prevalent in males

→More prevalent in females

Neuropsychological

Skin

Cause

[edit]
Adrenal Glands Zonations
SpecialtyEndocrinology, oncology Edit this on Wikidata
Adrenal Glands Zonations
SpecialtyEndocrinology, oncology Edit this on Wikidata

Study of the reported cases indicate that most adrenocortical adenomas occur due to neoplastic proliferation of adrenal cortical cells within the three distinct layers of adrenal cortex. In humans, the adrenal cortex comprises three concentric zones including the zona glomerulosa, zona fasciculata, and zona reticularis that under normal conditions respond to body's physiological demands for steroid hormones. The adrenal cortex is considered a dynamic organ in which senescent cells are replaced by newly differentiated cells. This constant renewal facilitates organ remodeling which contributes to dynamic characteristics of the adrenal cortex. [7] correspondingly, the developmental physiology of the adrenal cortex is believed to play a pivotal role in formation of the adrenocortical tumors. Hence, the molecular mechanisms involved in normal development of the adrenal glands are like double edged swords that can lead to the formation of tumors within the adrenal cortex. Moreover, recent studies suggest that mutations affecting the molecular pathways of the adrenocortical region can stimulate abnormal proliferation and tumor formation. Through these studies, the cyclic AMP-dependent protein kinase A signaling has been identified as a key mediator of cortisol secretion, and the mutations associated with the dysregulation of cyclic AMP - protein kinase A pathways have been implicated in the adrenocortical pathophysiology.[8]

Pathophysiology

[edit]

If functional, adrenocortical adenomas can affect the normal activities of the adrenal cortex. Located within the adrenal glands are the three zones that are responsible for secretion of the three major classes of adrenal steroids. Hence, functional adrenocortical adenomas can induce over-secretion of adrenal steroids associated with pure or mixed endocrine syndromes, a condition commonly known as hyperadrenalism.[citation needed]

Diagnosis

[edit]

Due to their asymptomatic nature, most reported cases of adrenal adenomas have been discerned fortuitously through autopsy, or during medical imaging, particularly CT scan (computed tomography) and magnetic resonance imaging. Hence, they have earned the title incidentaloma referring to small adenoma discovered incidentally.[9] Though adrenocortical adenomas are considered challenging to differentiate from the normal adrenal cortex, they appear as well-circumscribed lesions once isolated. [citation needed]

Imaging Diagnostics

Laboratory Tests

Gross Description

[edit]
  • Well-circumscribed lesion
  • Size ≤ 5 cm
  • Weight ≤ 50 grams
  • often appear as golden-yellow color mass

(may have focal dark regions corresponding to hemorrhage, lipid-depletion, and increased lipofuscin)[9]

Histopathology

[edit]
Zona fasciculata versus adrenocortical adenoma. An adrenocortical adenoma typically has mild changes in comparison, including larger cells with larger and more pleomorphic nuclei with more coarse chromatin. H&E stain.

The microscopic histopathology analysis of the tissue samples obtained from the adrenal cortex of individuals presenting with adenoma-associated symptoms such as primary aldestronism (PA) indicates that adenoma cells are relatively larger with different cytoplasm, and increased variation in nuclear size. This indication is based on comparison between the healthy (normal) and affected (adenoma-associated) adrenal cortex tissue samples. [citation needed]

  • Adrenocortical adenoma with focal high grade nuclear atypia
    Adrenocortical adenoma with focal high grade nuclear atypia
  • Adrenocortical adenoma with focal necrosis
    Adrenocortical adenoma with focal necrosis

Adrenocortical adenomas are most commonly distinguished from adrenocortical carcinomas (their malignant counterparts) by the Weiss system,[10] as follows:[11]

Characteristic[11] Score
High nuclear grade (enlarged, oval to lobated, with coarsely granular to hyperchromatic chromatin and easily discernible, prominent nucleoli)[12] 1
More mitoses than 5/50 high power fields 1
Atypical mitoses 1
Eosinophilic cytoplasm in >75% of tumor cells 1
Diffuse architecture of >33% of tumor 1
Necrosis 1
Venous invasion 1
Sinusoidal invasion (no smooth muscle in wall) 1
Capsular invasion 1

Total score indicates:[11]

  • 0-2: Adrenocortical adenoma
  • 3: Undetermined
  • 4-9: Adrenocortical carcinoma

Treatment

[edit]
  • Non-functioning cases of adrenocortical adenoma can be managed through long-term followups and monitoring.[citation needed]
  • The treatment approach for the functioning cases of adrenocortical adenoma depends on the type of disorders they induce and their advancement. Surgical excision may be required if its presence is resulting in atrophy of the adrenal glands and the surrounding tissues.[citation needed]

In order to acquire better treatment strategies, it is important to further examine, study and discern the distinct molecular mechanisms involved in the formation of endogenous Adrenal Adenomas, hyperplasias, and ACTH-independent Cushing's Syndrome to improve the available diagnostic and prognostic markers that can assist clinicians in the management and advance-treatment of such conditions.[13]

A 2018 Cochrane Systematic review compared two different types of surgery: laparoscopic retroperotenial adrenalectomy and laporoscopic transperitoenal adrenelectomy in different types of adrenal tumors.[14] Laparoscopic retroperotenial adrenalectomy appeared to reduce late morbility, time to oral fluid or food intake and time to ambulation, when compared to laparoscopic transperitoenal adrenalectomy.[14] However there was uncertainty in these findings due to low-quality evidence, as well as inconclusive findings about effects of either surgery on all-cause mortality, early morbidity, socioeconomic effects, duration of surgery, operative blood loss, conversion to open surgery.[14]

Prognosis

[edit]
  • The long-term outlook for individuals diagnosed with non-functional adrenocortical adenoma is usually excellent.
  • The long-term outlook for individuals diagnosed with functional adrenocortical adenoma is good with early diagnosis and treatment.

Epidemiology

[edit]
Incidences and prognoses of adrenal tumors,[15] with adrenocortical adenoma at left.
  • Prevalence: Female > Male
  • More common in adults
  • Relatively earlier onset in females (ages ≤ 20) than males (ages ≤ 30)
  • Most common cause of ACTH-independent Cushing's syndrome

See also

[edit]

References

[edit]
  1. ^ "Definition: adrenocortical adenoma from Online Medical Dictionary".
  2. ^ a b LaVoie, Melanie; Constantinides, Vasilis; Robin, Noel; Kyriacou, Angelos (30 July 2018). "Florid hyperandrogenism due to a benign adrenocortical adenoma". BMJ Case Reports. 2018: bcr-2018-224804. doi:10.1136/bcr-2018-224804. PMC 6067132. PMID 30061126.
  3. ^ Wang, Wei; Wei, Feng; Li, RanHao; Tian, JiaHui (October 2019). "A case report of idiopathic hyperaldosteronism characterized by bilateral adrenal adenoma". Medicine. 98 (43): e17418. doi:10.1097/MD.0000000000017418. PMC 6824822. PMID 31651844.
  4. ^ Ren, Kaiyun; Wei, Jia; Liu, Qilin; Zhu, Yuchun; Wu, Nianwei; Tang, Ying; Li, Qianrui; Zhang, Qianying; Yu, Yerong; An, Zhenmei; Chen, Jing; Li, Jianwei (17 June 2019). "Hypercortisolism and primary aldosteronism caused by bilateral adrenocortical adenomas: a case report". BMC Endocrine Disorders. 19 (1): 63. doi:10.1186/s12902-019-0395-y. PMC 6580498. PMID 31208392.
  5. ^ Kobayashi, Toshihiro; Imachi, Hitomi; Sato, Seisuke; Ibata, Tomohiro; Fukunaga, Kensaku; Yoshimoto, Takuo; Kikuchi, Fumi; Yonezaki, Kazuko; Yamaji, Nao; Lyu, Jingya; Dong, Tao; Nagata, Hiromi; Kadota, Kyuichi; Kushida, Yoshio; Haba, Reiji; Murao, Koji (1 February 2019). "Bilateral Adrenocortical Adenomas along with Virilization and Cushing's Syndrome". Internal Medicine. 58 (3): 405–409. doi:10.2169/internalmedicine.0790-18. PMC 6395137. PMID 30210105.
  6. ^ Rodríguez-Gutiérrez, René; Bautista-Medina, Mario Arturo; Teniente-Sanchez, Ana Eugenia; Zapata-Rivera, Maria Azucena; Montes-Villarreal, Juan (2013). "Pure Androgen-Secreting Adrenal Adenoma Associated with Resistant Hypertension". Case Reports in Endocrinology. 2013: 356086. doi:10.1155/2013/356086. PMC 3681270. PMID 23819074.
  7. ^ Pihlajoki, Marjut; Dörner, Julia; Cochran, Rebecca S.; Heikinheimo, Markku; Wilson, David B. (5 March 2015). "Adrenocortical Zonation, Renewal, and Remodeling". Frontiers in Endocrinology. 6: 27. doi:10.3389/fendo.2015.00027. PMC 4350438. PMID 25798129.
  8. ^ Lodish, Maya (June 2017). "Genetics of Adrenocortical Development and Tumors". Endocrinology and Metabolism Clinics of North America. 46 (2): 419–433. doi:10.1016/j.ecl.2017.01.007. PMC 5424622. PMID 28476230.
  9. ^ a b Lloyd, Ricardo V. (April 2011). "Adrenal cortical tumors, pheochromocytomas and paragangliomas". Modern Pathology. 24: S58–65. doi:10.1038/modpathol.2010.126. PMID 21455202.
  10. ^ Wang, Cuiping; Sun, Yang; Wu, Huanwen; Zhao, Dachun; Chen, Jie (2014). "Distinguishing adrenal cortical carcinomas and adenomas: a study of clinicopathological features and biomarkers". Histopathology. 64 (4): 567–576. doi:10.1111/his.12283. ISSN 0309-0167. PMC 4282325. PMID 24102952.
  11. ^ a b c Aye, Than Than; Myint, Phone; Myint, Kyar Nyo Soe (2015). "Adrenocortical Oncocytoma Presenting with Gynaecomastia". Journal of the ASEAN Federation of Endocrine Societies. 30 (1): 27–30. doi:10.15605/jafes.030.01.08. ISSN 0857-1074.
  12. ^ Tito Fojo (26 December 2016). "Adrenocortical Cancer". Retrieved 2020-07-02.
  13. ^ Bourdeau, Isabelle; Lampron, Antoine; Costa, Marcia Helena Soares; Tadjine, Mimi; Lacroix, André (June 2007). "Adrenocorticotropic hormone-independent Cushing's syndrome". Current Opinion in Endocrinology, Diabetes and Obesity. 14 (3): 219–225. doi:10.1097/MED.0b013e32814db842. PMID 17940443. S2CID 40454423.
  14. ^ a b c Arezzo, Alberto; Bullano, Alberto; Cochetti, Giovanni; Cirocchi, Roberto; Randolph, Justus; Mearini, Ettore; Evangelista, Andrea; Ciccone, Giovannino; Bonjer, H. Jaap; Morino, Mario (2018-12-30). Cochrane Metabolic and Endocrine Disorders Group (ed.). "Transperitoneal versus retroperitoneal laparoscopic adrenalectomy for adrenal tumours in adults". Cochrane Database of Systematic Reviews. 2018 (12): CD011668. doi:10.1002/14651858.CD011668.pub2. PMC 6517116. PMID 30595004.
  15. ^ Data and references for pie chart are located at file description page in Wikimedia Commons.
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Adrenocortical_adenoma&oldid=1236571491"