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Leydig cell tumour


Source: http://en.wikipedia.org/wiki/Leydig_cell_tumour
Updated: 2017-08-30T12:33Z
Leydig cell tumour
Leydig cell tumour1.jpg
Low magnification micrograph of a Leydig cell tumour. H&E stain.
Classification and external resources
Specialty{{#statements:P1995}}
ICD-9-CM183.0, 256.1
ICD-O8631
DiseasesDB7445
MedlinePlus000409
Patient UKLeydig cell tumour
MeSHD007984
[[[d:Lua error in Module:Wikidata at line 1016: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]

Leydig cell tumour, also Leydig cell tumor (US spelling), (testicular) interstitial cell tumour and (testicular) interstitial cell tumor (US spelling), is a member of the sex cord-stromal tumour group[1] of ovarian and testicular cancers. It arises from Leydig cells. While the tumour can occur at any age, it occurs most often in young adults.

A Sertoli-Leydig cell tumour is a combination of a Leydig cell tumour and a Sertoli cell tumour from Sertoli cells.

Presentation

The majority of Leydig cell tumors are found in males, usually at 5–10 years of age or in middle adulthood (30–60 years). Children typically present with precocious puberty. Due to excess testosterone secreted by the tumour, one-third of female patients present with a recent history of progressive masculinization. Masculinization is preceded by anovulation, oligomenorrhea, amenorrhea and defeminization. Additional signs include acne and hirsutism, voice deepening, clitoromegaly, temporal hair recession, and an increase in musculature. Serum testosterone level is high.[citation needed]

In men testicular swelling is the most common presenting feature. Other symptoms depend on their age and the type of tumour. If it is secreting androgens the tumour is usually asymptomatic, but can cause precocious puberty in pre-pubertal boys. If the tumour secretes oestrogens it can cause feminisation in young boys. In adults, this causes a number of problems including gynaecomastia, erectile dysfunction, infertility, feminine hair distribution, gonadogenital atrophy, and a loss of libido.[2]

Cause

Diagnosis

Presence of an ovarian tumour plus hormonal disturbances suggests a Leydig cell tumour, granulosa cell tumour or thecoma. However, hormonal disturbances, in Leydig tumours, is present in only 2/3 of cases. Testicular Leydig cell tumours can be detected sonographically, ultrasound examinations may be ordered in the event of a palpable scrotal lump, however incidental identification of these lesions is also possible[3].

A conclusive diagnosis is made via histology, as part of a pathology report made during or after surgery. Reinke crystals are classically found in these tumours and help confirm the diagnosis, although they are seen in less than half of all Leydig cell tumours. See also Sex cord-stromal tumour. Immunohistochemical markers of Leydig cell tumours include inhibin-alpha, calretinin, and melan-A.[4]

Treatment

The usual chemotherapy regimen has limited efficacy in tumours of this type, although Imatinib has shown some promise.[5] There is no current role for radiotherapy.[6]

The usual treatment is surgery. The surgery for females usually is a fertility-sparing unilateral salpingo-oophorectomy. For malignant tumours, the surgery may be radical and usually is followed by adjuvant chemotherapy, sometimes by radiation therapy. In all cases, initial treatment is followed by surveillance. Because in many cases Leydig cell tumour does not produce elevated tumour markers,[7] the focus of surveillance is on repeated physical examination and imaging.

In males, a radical inguinal orchiectomy is typically performed. However, testes-sparing surgery can be used to maintain fertility in children and young adults. This approach involves an inguinal or scrotal incision and ultrasound guidance if the tumour is non-palpable. This can be done because the tumour is typically unifocal, not associated with precancerous lesions, and is unlikely to recur.[8]

The prognosis is generally good as the tumour tends to grow slowly and usually is benign: 10% are malignant.[2][9] For malignant tumours with undifferentiated histology, prognosis is poor.[7]

Additional images

See also

References

  1. ^ Sachdeva P, Arora R, Dubey C, Sukhija A, Daga M, Singh DK (April 2008). "Sertoli-Leydig cell tumor: a rare ovarian neoplasm. Case report and review of literature". Gynecol. Endocrinol. 24 (4): 230–4. PMID 18382911. doi:10.1080/09513590801953465. 
  2. ^ a b "Leydig Cell Tumors: Practice Essentials, Background, Pathophysiology". 2016-10-27. 
  3. ^ Reddan, Tristan; Powell, Jennifer; Long, Gillian (2017). "Ultrasound of a prepubertal Leydig cell tumour of the testis". Sonography. doi:10.1002/sono.12111. Retrieved 5 June 2017. 
  4. ^ Ulbright TM, Srigley JR, Hatzianastassiou DK, Young RH (November 2002). "Leydig cell tumors of the testis with unusual features: adipose differentiation, calcification with ossification, and spindle-shaped tumor cells". Am. J. Surg. Pathol. 26 (11): 1424–33. PMID 12409718. doi:10.1097/00000478-200211000-00004. 
  5. ^ "Medscape Log In". reference.medscape.com. Retrieved 2016-12-06. 
  6. ^ "Leydig Cell Tumors Treatment & Management: Medical Care, Surgical Care". 2016-10-27. 
  7. ^ a b Lenhard M, Kuemper C, Ditsch N, Diebold J, Stieber P, Friese K, Burges A (2007). "Use of novel serum markers in clinical follow-up of Sertoli-Leydig cell tumours". Clin. Chem. Lab. Med. 45 (5): 657–61. PMID 17484630. doi:10.1515/CCLM.2007.120. 
  8. ^ Ferretti L, Sargos P, Gross-Goupil M, Izard V, Wallerand H, Huyghe E, Rigot JM, Durand X, Benoit G, Ferriere JM, Droupy S (2014). "Testicular-sparing surgery for bilateral or monorchide testicular tumours: a multicenter study of long-term oncological and functional results.". BJU Int. 
  9. ^ Al-Agha OM, Axiotis CA (February 2007). "An in-depth look at Leydig cell tumor of the testis". Arch. Pathol. Lab. Med. 131 (2): 311–7. PMID 17284120. doi:10.1043/1543-2165(2007)131[311:AILALC]2.0.CO;2. 
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